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Pre-incision Versus Lapaorscopic-assisted Transversus Abdominis Plane (TAP) and Rectus Sheath Block for Post-Cholecystectomy Pain

Primary Purpose

Post Operative Pain

Status
Enrolling by invitation
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block
Sponsored by
Patel Hospital, Pakistan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post Operative Pain

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Age above 18 to 75 years, both genders, Elective Laparoscopic Cholecystectomies, American Society of Anesthesiologists (ASA) physical status I & II, Give consent. Exclusion Criteria: o History of allergy , hypersentivity or contraindication to Rupivacaine, nalbuphine ,Paracetamol. Local skin allergy Laparoscopic converted to open Previous open upper abdominal or midline surgeries Diagnosis Of "Chronic Pain Syndrome" Known Alcohol Or Substance Abuse Within The Last 6 Months Anti-psychotic, antidepressants, steroids use Multiple procedures planned under single GA Pregnancy Unable to understand i.e. deaf, language barrier, mentally incapacitated Coagulopathy

Sites / Locations

  • Patel Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Pre-incision TAP (PITAP) and Rectus Sheath block

Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block

Arm Description

Pre-incision TAP block and Rectus sheath block will be performed after induction of anesthesia, just after prep and drape by Blind double pop technique by Anesthetist/Anesthesia trainee.Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be Immediate right subcostal region , 3 cm medially to mid axillary line The intervention and the control group will receive TAP block and rectus sheath block with Rupivacaine (3mg/kg). 1 ampule is of 10 ml and consists of 50mg /10ml, maximum dose will be 300mg. will use a of minimum volume of solution 50ml which will be made by 3 ampules of Rupivacaine and it will be diluted to a total of 20ml of injectate( distilled water )which is then divided between the four rectus block sites (5ml each) and one TAP block site(30ml ).

Laparoscopic -assisted TAP and rectus sheath block will be performed after insertion of optical port By Surgeon /surgery trainee.Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be Immediate right subcostal region , 3 cm medially to mid axillary line The intervention and the control group will receive TAP block and rectus sheath block with Rupivacaine (3mg/kg). 1 ampule is of 10 ml and consists of 50mg /10ml, maximum dose will be 300mg. will use a of minimum volume of solution 50ml which will be made by 3 ampules of Rupivacaine and it will be diluted to a total of 20ml of injectate( distilled water )which is then divided between the four rectus block sites (5ml each) and one TAP block site(30ml each).

Outcomes

Primary Outcome Measures

Post-operative pain changes
post operative chnage of pain score assessment at 3,6,12,24 hrs at resting and coughing. Pain score will be assessed using VAS score

Secondary Outcome Measures

Rescue analgesia need
if any additional anlagesia is required , nalbuphine 2mg IV as per need will be used via PCA pump.
Visceral Injury
if any viscera is damage during TAP and rectus sheath block in both groups
Peritoneal injury
• Peritoneal entry will be seen under laparoscopic vision. For LATAP ,entry would be labelled when tip of needle will be seen piercing peritoneum and for PITAP any erythema or bleed at the site of entry seen under laparoscopic vision.
TAP and rectus sheath block timings
comparsion of timings between both groups ,• Timings of PITAP AND LATAP will be noted in seconds by putting the timer on at the start of the procedures when anesthesia/surgery team calls the procedure on and by putting the timer off ,when they calls the procedure off.

Full Information

First Posted
April 21, 2023
Last Updated
May 3, 2023
Sponsor
Patel Hospital, Pakistan
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1. Study Identification

Unique Protocol Identification Number
NCT05856682
Brief Title
Pre-incision Versus Lapaorscopic-assisted Transversus Abdominis Plane (TAP) and Rectus Sheath Block for Post-Cholecystectomy Pain
Official Title
Pre-incision Versus Lapaorscopic-assisted Transversus Abdominis Plane (TAP) and Rectus Sheath Block for Post-Cholecystectomy Pain Management: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
July 1, 2022 (Actual)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
August 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Patel Hospital, Pakistan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this clinical trial is to compare pre-incision vs laparoscopic assisted Transversus abdominis plane and rectus sheath block in patients undergoing laparoscopic cholecystectomy. The main question it aims to answer is: • if the effectiveness of TAP and rectus sheath block varies according to whether it is performed pre-incisional (pre emptive) or intraoperatively under Laparoscopic vision for laparoscopic cholecystectomies. Participants will be assessed for pain at 3,6,12, and 24 hrs after surgery. Researchers will compare pain score between Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block vs Pre-incision TAP (PITAP ) .
Detailed Description
INTRODUCTION: Every year Over 13 million Laparoscopic procedures are performed globally. In the USA, 90% of the cholecystectomies are performed with the laparoscopic technique Laparoscopic cholecystectomy is the gold standard in many health centers as it is less invasive compared to open cholecystectomy. Good post-operative pain control, not only prevents post-operative complications but is also essential for early ambulation and return to daily routine. It is important to keep side effects minimum besides pain relieve. Therefore pre-emptive wound analgesia has been popularized. Preemptive analgesia(for eg: TAP block) is defined as an anti-nociceptive treatment that is initiated before the surgical procedure in order to reduce the sensitization (occurs because of transmission of pain signals evoked by tissue damage) of the peripheral and central pain pathways. Some analyses have shown no beneficial effect(4) whereas some have failed to reach a final conclusion regarding efficacy of pre-emptive analgesia. For post-laparoscopic pain management ,a multimodal approach with non-steroidal anti-inflammatory drugs, opioids and loco-regional techniques have been recommended . The Transversus Abdominis Plane (TAP) block is an analgesia technique that is loco-regional ,consists of infiltrating a local anesthetic solution between the plane of the Transversus abdominis muscle and the internal oblique muscle. TAP block has gradually become an alternative postoperative analgesia technology and it was described in 2001 by Rafi. . Several techniques are currently used to deliver TAP blocks, including blinded double pop technique, ultrasound-guided and laparoscopic-assisted approaches. The latter was first described in 2011 by Chetwood et al. while performing laparoscopic nephrectomies . The advantages of this technique include ease of performance, less dependency on specialized skill set or equipment, time efficient, less risk of visceral injury and avoidance of intraperitoneal local anaesthetic infiltration . RATIONALE: Many studies have demonstrated the therapeutic benefit of laparoscopic-assisted TAP block in initial post-operative pain management in comparision with periportal local anaesthetic infiltration for patients undergoing elective laparoscopic procedures(for eg; for laparoscopic hernia repair). To the best of our knowledge, there is a paucity of data since laparoscopic-assisted TAP block has not been utilized or evaluated prospectively to see if the effectiveness of TAP block varies according to whether it is performed pre-incisional (pre emptive) or intraoperatively under Laparoscopic vision for laparoscopic cholecystectomies. Moreover, the rectus sheath block in conjunction with TAP block has not been evaluated before. OBJECTIVE : To compare the mean post-operative pain score at (3, 6, 12, 24 hours) with pre-incision versus laparoscopic-assisted Transversus Abdominis Plane (TAP) and Rectus sheath block in patients undergoing Laparoscopic cholecystectomy at a tertiary care hospital. HYPOTHESIS : Post-Cholecystectomy pain control after Laparoscopic-assisted TAP block is not inferior to pain control after pre-incisional TAP block. OPERATIONAL DEFINITIONS : Transversus abdominis plane(TAP block): It is a regional analgesia technique which involves the injection of a local anesthetic solution into a plane between the internal oblique muscle and transversus abdominis muscle. Since the thoracolumbar nerves originating from the T6 to L1 spinal roots run into this plane and supply sensory nerves to the antero-lateral abdominal wall , the local anesthetic spread in this plane can block the neural afferents and provide analgesia to the antero-lateral abdominal wall. Rectus sheath block : It is a method of trunk analgesia most useful for midline surgical procedures at or above the umbilicus. Local anesthetic is injected at the lateral edge of the rectus sheath where branches of the intercostal nerves enter. Instillation of local anesthetic bilaterally between the rectus muscle and the posterior sheath provides midline analgesia for several dermatomes around the injection site. Pain score (visual analogue scale): The Visual Analogue Scale (VAS) is the standard tool for rating of pain - either patient's own rating or rated by the health care worker. The visual analog scale is a straight line from 1 to 10 with one end meaning no pain and the other end meaning the worst pain. A patient marks a point on the line that matches the intensity of pain he or she feels. MATERIALS AND METHODS: STUDY DESIGN: Double blinded, Randomized controlled trial SETTINGS: The study will be conducted at the department of General Surgery, Patel hospital Karachi. DURATION OF STUDY: After ERC approval, minimum Six months or till the sample size is achieved. RANDOMIZATION: Computer generated randomization table with blocks of four. Co-ordinator of HEC will have the table. BLINDING: Double blinded (Patient, Person assessing post-operative pain will be blinded to the both groups). INTERVENTION GROUP: Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block CONTROL GROUP: Pre-incision TAP (PITAP) block by Anesthesist. SAMPLE SIZE : In each arm, 112 patients. SAMPLE CALCULATION METHOD: Calculated using WHO software. Power set as =90% Confidence interval =95% Level of significance = 5% SAMPLING TECHNIQUE: Purposive, non probability DATA COLLECTION PROCEDURE: Study will be started after approval by the institutional ethical committee. Detailed history, examination and relevant investigations of patients will be performed. Informed and written consent will be taken. Proforma will be filled for patients undergoing planned surgery fulfilling the inclusion criteria . Anesthesia will be standardized in all patients. All patients will receive paracetamol 1000 mg and nalbuphine 0.15mg/kg after induction of anaesthesia. Both the procedures will be performed by either Resident(having experience of procedure) or consultant himself/herself. Syringes will be prepared by one of the research team member for each patient in a designated sterile area on the day of surgery.. Pre-incision TAP block and Rectus sheath block will be performed after induction of anesthesia, just after prep and drape by Blind double pop technique by Anesthetist/Anesthesia trainee Laparoscopic -assisted TAP and rectus sheath block will be performed after insertion of optical port By Surgeon /surgery trainee Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be Immediate right subcostal region , 3 cm medially to mid axillary line . The intervention and the control group will receive TAP block and rectus sheath block with Rupivacaine (3mg/kg). 1 ampule is of 10 ml and consists of 50mg /10ml, maximum dose will be 300mg. We will use a of minimum volume of solution 50ml which will be made by 3 ampules of Rupivacaine and it will be diluted to a total of 20ml of injectate( distilled water )which is then divided between the four rectus block sites (5ml each) and one TAP block site(30ml). Needle used for the blocks will be of 25guage and tip of the needle will be blunted by gentle tapping on metallic surface. Syringe will be of 50ml . Timings of PITAP AND LATAP will be noted in seconds by putting the timer on at the start of the procedures when anesthesia/surgery team calls the procedure on and by putting the timer off ,when they calls the procedure off. Peritoneal entry will be seen under laparoscopic vision. For LATAP ,entry would be labelled when tip of needle will be seen piercing peritoneum and for PITAP any erythema or bleed at the site of entry seen under laparoscopic vision. Visceral entry will be seen under laparoscopic vision for both LATAP and PITAP. Diet will be Regular and started after 6 hours of the surgery. Ambulation will be started as soon as patient is awake . Antibiotics (cefazolin 1gm ,q8hrly) will be prescribed post-operatively to contaminated surgery. Patient-controlled analgesia(PCA) will be given in the post-operative period for all patients for rescue analgesia and explained to them pre-operatively. On having pain, as per need , Patient will press the button on a pump that is connected to IV catheter. Patient will receive a preset dose of Nalbuphine 2mg. Pain assessment will be measured using the visual analogue scale (0-10). Pain will be assessed at both rest and coughing (reflect pain induced by physical activity) at 3,6,12, and 24 hrs after surgery by an observer blinded to both intervention and control group. DATA ANALYSIS plan: SPSS (ver. 16) will be used for data analysis. Confounding and effect modifying variables i.e. age, sex, diabetes are analyzed by multiple linear regression. For Data that will follow normality Independent sample T test will be applied, for data that will not follow normality Mann- whitney u test will be applied. P-value of less than 0.05 is considered statistically significant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post Operative Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
randomized, prospective, double blinded
Masking
ParticipantOutcomes Assessor
Masking Description
Double blinded study : participants and person assessing the post operative pain will be blinded to both the control and intervention group, person performing TAP block will not be assessing the outcome
Allocation
Randomized
Enrollment
224 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pre-incision TAP (PITAP) and Rectus Sheath block
Arm Type
Active Comparator
Arm Description
Pre-incision TAP block and Rectus sheath block will be performed after induction of anesthesia, just after prep and drape by Blind double pop technique by Anesthetist/Anesthesia trainee.Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be Immediate right subcostal region , 3 cm medially to mid axillary line The intervention and the control group will receive TAP block and rectus sheath block with Rupivacaine (3mg/kg). 1 ampule is of 10 ml and consists of 50mg /10ml, maximum dose will be 300mg. will use a of minimum volume of solution 50ml which will be made by 3 ampules of Rupivacaine and it will be diluted to a total of 20ml of injectate( distilled water )which is then divided between the four rectus block sites (5ml each) and one TAP block site(30ml ).
Arm Title
Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block
Arm Type
Active Comparator
Arm Description
Laparoscopic -assisted TAP and rectus sheath block will be performed after insertion of optical port By Surgeon /surgery trainee.Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be Immediate right subcostal region , 3 cm medially to mid axillary line The intervention and the control group will receive TAP block and rectus sheath block with Rupivacaine (3mg/kg). 1 ampule is of 10 ml and consists of 50mg /10ml, maximum dose will be 300mg. will use a of minimum volume of solution 50ml which will be made by 3 ampules of Rupivacaine and it will be diluted to a total of 20ml of injectate( distilled water )which is then divided between the four rectus block sites (5ml each) and one TAP block site(30ml each).
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block
Other Intervention Name(s)
Pre-incision TAP (PITAP) and Rectus Sheath block
Intervention Description
Laparoscopic -assisted TAP and rectus sheath block will be performed after insertion of optical port By Surgeon /surgery trainee. • Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be anterior to the midaxillary line between the costal margin and iliac crest bilaterally.
Primary Outcome Measure Information:
Title
Post-operative pain changes
Description
post operative chnage of pain score assessment at 3,6,12,24 hrs at resting and coughing. Pain score will be assessed using VAS score
Time Frame
3,6,12,24 hrs post-operatively
Secondary Outcome Measure Information:
Title
Rescue analgesia need
Description
if any additional anlagesia is required , nalbuphine 2mg IV as per need will be used via PCA pump.
Time Frame
Post operatively at 3,6,12,24hrs
Title
Visceral Injury
Description
if any viscera is damage during TAP and rectus sheath block in both groups
Time Frame
at the time of surgery
Title
Peritoneal injury
Description
• Peritoneal entry will be seen under laparoscopic vision. For LATAP ,entry would be labelled when tip of needle will be seen piercing peritoneum and for PITAP any erythema or bleed at the site of entry seen under laparoscopic vision.
Time Frame
at the time of surgery
Title
TAP and rectus sheath block timings
Description
comparsion of timings between both groups ,• Timings of PITAP AND LATAP will be noted in seconds by putting the timer on at the start of the procedures when anesthesia/surgery team calls the procedure on and by putting the timer off ,when they calls the procedure off.
Time Frame
at the time of surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age above 18 to 75 years, both genders, Elective Laparoscopic Cholecystectomies, American Society of Anesthesiologists (ASA) physical status I & II, Give consent. Exclusion Criteria: o History of allergy , hypersentivity or contraindication to Rupivacaine, nalbuphine ,Paracetamol. Local skin allergy Laparoscopic converted to open Previous open upper abdominal or midline surgeries Diagnosis Of "Chronic Pain Syndrome" Known Alcohol Or Substance Abuse Within The Last 6 Months Anti-psychotic, antidepressants, steroids use Multiple procedures planned under single GA Pregnancy Unable to understand i.e. deaf, language barrier, mentally incapacitated Coagulopathy
Facility Information:
Facility Name
Patel Hospital
City
Karachi
State/Province
Sindh
ZIP/Postal Code
75300
Country
Pakistan

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31523579
Citation
Amreek F, Hussain SZM, Mnagi MH, Rizwan A. Retrospective Analysis of Complications Associated with Laparoscopic Cholecystectomy for Symptomatic Gallstones. Cureus. 2019 Jul 16;11(7):e5152. doi: 10.7759/cureus.5152.
Results Reference
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PubMed Identifier
19911275
Citation
Csikesz NG, Singla A, Murphy MM, Tseng JF, Shah SA. Surgeon volume metrics in laparoscopic cholecystectomy. Dig Dis Sci. 2010 Aug;55(8):2398-405. doi: 10.1007/s10620-009-1035-6. Epub 2009 Nov 13.
Results Reference
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Citation
Ortiz J, Rajagopalan S. A review of local anesthetic techniques for analgesia after laparoscopic surgery. J Minim Invasive Surg Sci. 2014;3:e11310
Results Reference
background
PubMed Identifier
29226150
Citation
Tsai HC, Yoshida T, Chuang TY, Yang SF, Chang CC, Yao HY, Tai YT, Lin JA, Chen KY. Transversus Abdominis Plane Block: An Updated Review of Anatomy and Techniques. Biomed Res Int. 2017;2017:8284363. doi: 10.1155/2017/8284363. Epub 2017 Oct 31.
Results Reference
background
PubMed Identifier
11576144
Citation
Rafi AN. Abdominal field block: a new approach via the lumbar triangle. Anaesthesia. 2001 Oct;56(10):1024-6. doi: 10.1046/j.1365-2044.2001.02279-40.x. No abstract available.
Results Reference
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PubMed Identifier
18020088
Citation
Hebbard P, Fujiwara Y, Shibata Y, Royse C. Ultrasound-guided transversus abdominis plane (TAP) block. Anaesth Intensive Care. 2007 Aug;35(4):616-7. No abstract available.
Results Reference
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PubMed Identifier
25899736
Citation
Elamin G, Waters PS, Hamid H, O'Keeffe HM, Waldron RM, Duggan M, Khan W, Barry MK, Khan IZ. Efficacy of a Laparoscopically Delivered Transversus Abdominis Plane Block Technique during Elective Laparoscopic Cholecystectomy: A Prospective, Double-Blind Randomized Trial. J Am Coll Surg. 2015 Aug;221(2):335-44. doi: 10.1016/j.jamcollsurg.2015.03.030. Epub 2015 Mar 27.
Results Reference
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PubMed Identifier
21401554
Citation
Chetwood A, Agrawal S, Hrouda D, Doyle P. Laparoscopic assisted transversus abdominis plane block: a novel insertion technique during laparoscopic nephrectomy. Anaesthesia. 2011 Apr;66(4):317-8. doi: 10.1111/j.1365-2044.2011.06664.x. No abstract available.
Results Reference
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PubMed Identifier
30173291
Citation
Mughal A, Khan A, Rehman J, Naseem H, Waldron R, Duggan M, Khan W, Barry K, Khan IZ. Laparoscopic-assisted transversus abdominis plane block as an effective analgesic in total extraperitoneal inguinal hernia repair: a double-blind, randomized controlled trial. Hernia. 2018 Oct;22(5):821-826. doi: 10.1007/s10029-018-1819-8. Epub 2018 Sep 1. Erratum In: Hernia. 2018 Sep 21;:
Results Reference
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Citation
Chapter 57 - Rectus Sheath Block, Editor(s): Andrew T. Gray, Atlas of Ultrasound-Guided Regional Anesthesia (Third Edition),Elsevier, 2019,Pages 249-258,ISBN 9780323509510.
Results Reference
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PubMed Identifier
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Citation
Delgado DA, Lambert BS, Boutris N, McCulloch PC, Robbins AB, Moreno MR, Harris JD. Validation of Digital Visual Analog Scale Pain Scoring With a Traditional Paper-based Visual Analog Scale in Adults. J Am Acad Orthop Surg Glob Res Rev. 2018 Mar 23;2(3):e088. doi: 10.5435/JAAOSGlobal-D-17-00088. eCollection 2018 Mar.
Results Reference
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Links:
URL
http://idataresearch.com/over-13-million-laparoscopic-procedures-are-performed-globally-every-year/
Description
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Pre-incision Versus Lapaorscopic-assisted Transversus Abdominis Plane (TAP) and Rectus Sheath Block for Post-Cholecystectomy Pain

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