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To Compare the Skin Incision Made by the Electrocautery and Scalpel in Inguinal Hernia Repair

Primary Purpose

Post-operative Pain, Acute

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Open Mesh Hernioplasty
Sponsored by
Tribhuvan University Teaching Hospital, Institute Of Medicine.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post-operative Pain, Acute

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients ≥ 18 years old who are operated with the diagnosis of inguinal hernia. Exclusion Criteria: Patients with recurrent inguinal hernia Patients presenting with incarcerated, irreducible and strangulated hernia Bilateral Inguinal Hernia Patient taking steroids Patient with contraindication to NSAIDs such as CKD, Drug hypersensitivity etc Patients who do not give written consent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    Group 1: Scalpel

    Group 2 : Electrocautery

    Arm Description

    Skin Incision for inguinal hernia repair will be given by Stainless steel blade no.10. Open Mesh Hernioplasty

    Open Mesh Hernioplasty Skin Incision for inguinal hernia repair will be given by following: Cautery machine: Erbe VIO 300 S Cut setting: Cut:30 Coagulate:30 Cautery tip (tip pointed) Mode: Monopolar

    Outcomes

    Primary Outcome Measures

    To Compare the incidence of post-operative pain between two groups.
    For assessment of pain; visual analog scale will be used in every patients.

    Secondary Outcome Measures

    To compare the post-operative analgesic dose requirement between the two groups.
    For assessment of analgesic dose requirement; will be asked using the telephone conversation.
    To Compare the incidence of other complications like SSI, Hematoma, Seroma and Urinary retention between the two groups.
    For assessment of other post-operative complications ; patient will be followed up in OPD after telephone conversation.

    Full Information

    First Posted
    December 15, 2022
    Last Updated
    January 7, 2023
    Sponsor
    Tribhuvan University Teaching Hospital, Institute Of Medicine.
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05666973
    Brief Title
    To Compare the Skin Incision Made by the Electrocautery and Scalpel in Inguinal Hernia Repair
    Official Title
    A Comparative Study on Electrocautery Versus Scalpel for Skin Incision in Inguinal Hernia Repair : A Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    January 2023 (Anticipated)
    Primary Completion Date
    April 2023 (Anticipated)
    Study Completion Date
    April 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Tribhuvan University Teaching Hospital, Institute Of Medicine.

    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 Groin hernia repair is a commonly performed general surgery procedure in both adults and children with inguinal hernias constituting more than 95% of all groin hernia repairs. Inguinal hernia repair is a commonly performed surgical procedure in our part of the world and is one of the common cause of hospital admission from the emergency or out patient department. Traditionally, surgical skin incisions have been made with surgical scalpel while modern method of making incisions with electrocautery had made it more sharp, precise and less time consuming. The cases of inguinal hernia are being managed in our center, Tribhuvan University Teaching Hospital. Generally, these patients are seen by the residents and supervised by the faculties in the emergency and in OPD and later if required admitted in the wards. Clinical examination and imaging are done for the diagnosis . Then severity assessment is performed and the management is done accordingly. The proposed study will be a hospital based comparative study and aims to observe the overview of the surgical management of OPD based day care surgery of inguinal hernia and also to observe whether the surgical incision is being performed with scalpel or electrocautery. The patients fulfilling the inclusion criteria are selected for the study. Sample will be selected by non-probability (convenience) method and study variables will be recorded in proforma. Statistical analysis will be done using SPSS version 23. Results obtained from the study will be reviewed and discussed with published literature.
    Detailed Description
    Inguinal hernia is formed by the protrusion of the peritoneum with its contents through an opening; and the contents - that is, any tissue or organ that protrudes through the neck into the hernia sac. The inguinal hernias are either direct or indirect and both types of hernias protrude above the inguinal ligament.1 Incision is a cut or slit to gain access to underlying structures . Cauterization is a medical term describing burning of body skin to remove or close a part of it. Electrocautery is used increasingly for tissue dissection, although fears of excessive scarring and poor wound healing have curtailed its widespread use for skin incision.2 Traditionally, surgical skin incisions have been made with steel blade. This method of making skin incision is an old method and surgeons have always been in search of some new methods for making surgical skin incisions because incision made by scalpel were supposed to be more bloody, time consuming and more painful.3 Electrocautery which is available in all surgical theaters is less frequently used for skin incisions for the fear of tissue damage, fear of post operative pain and scarring. Recent advances and studies have shown that electrocautery can be used for skin incision without any postoperative complications like wound infection and scarring and less post operative pain.4,5 It has now become an integral and evolving part of surgical practice. However, most surgeons still make skin incision with a scalpel and divide the deeper structures with coagulation diathermy. Modern surgical scalpels are usually made of hardened steel for better sharpness and precision. Basic scalpel design has remained almost the same but there has been a substantial improvement in the electrosurgical instruments.5 Fear of deep burns with diathermy and the resultant scarring continues compared with the scalpel, which produces a clean, incised wound with minimal tissue destruction. Cutting diathermy incision with an electrode delivering pure sinusoidal current allows tissue cleavage by rapid cell vaporization without damage to surrounding areas. This may explain the absence of tissue charring and subsequent healing with minimal scarring. Cutting diathermy can make hemostasis quicker and satisfactory, save the operative time, and can produce an incised wound that heals like the one created by cold scalpel.6,7 Many other studies have been conducted to compare electrocautery skin incision over scalpel skin incision in terms of time taken for incision, postoperative pain and wound healing especially in cases of inguinal hernia surgery, some have reported that the use of diathermy for skin incision during inguinal hernioplasty is as safe as the use of scalpel in terms of wound healing .4 There are other studies which reported that the use of diathermy reduces the use of analgesics requirements in the postoperative period. But still, some studies have reported that the postoperative analgesic requirement are similar in both the techniques and likewise postoperative complications. This study is undertaken to alleviate the fear of using electrocautery for skin incisions in surgical community. Patients with the provisional diagnosis of inguinal hernia were seen by the residents and supervised by the faculty in the emergency. The severity grading of those patients were done and later admitted in the ward for further management accordingly. Field Block(Infiltration): Anesthetic agent: Local: Lidoocaine hydrochloride 2% with Adrenaline 1:2,00,000 Each ml ;Lidocaine 20mg, Adrenaline 5mcg Maximum safe dose: 7mg/kg (maximum 500mg;25 ml) Local Bupivacaine hydrochloride 0.5% Each ml ;Bupivacaine hydrochloride 5 mg Maximum safe dose: 3mg/kg (maximum 225mg;45 ml) Local Anesthesia: - Field block : With 20 ml Lidocaine 2% and 10 ml Bupivacaine 0.5 % mixed with 20 ml Normal Saline and infiltration in the desired field done. Steps of surgery: Injection Ceftriaxone 50 mg/kg iv stat dose will be given pre-operatively Incision: medial 3/5 and 2.5 cms above and parallel to inguinal ligament extending from pubic tubercle upto 1 cm lateral to mid point of inguinal ligament. Group 1- Incision with scalpel , bleeding controlled by forcep coagulation. Group 2- Incision with electro cautery needle, hemostasis will be achieved with electrocautery coagulation. Cut the subcutaneous tissues,external oblique aponeurosis opened in layers Nerve Iliohypogastric & ilioinguinal will be preserved (by taking aside from the field) Intra-operative Injection Tramadol(50 mg) and ondansetron(4 mg) iv stat dose given Sac ligated with Polygalactin 2-0 suture. Lichtenstein method of repair Mesh type: large pore polypropylene mesh Mesh size: 3 x 6 inches(7.5 x 15 cms) Mesh Fixation: polypropylene 2-0 External oblique closure Skin closure: Ethilon 2 - 0 suture Postoperative: Antibiotic: Tab. Cefixime 200 mg PO x BD x 5 days Analgesic : Tab Paracetamol 1gm PO x QID x 3 days and SOS Tab ketorolac 10 mg PO x SOS Tab Pantoprazole 40 mg PO x OD x 5 days The medical records including vital signs, laboratory data, medications and physical examination findings of patients would be reviewed throughout their hospitalization period.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Post-operative Pain, Acute

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Participants are assigned to study where two groups of treatments Group 1 (Scalpel) and Group 2 (Electrocautery) are given so that Group 1 will receive skin incision only by Scalpel and another group will receive skin incision by Electrocautery for the duration of study.
    Masking
    ParticipantInvestigator
    Masking Description
    Patients will be randomly distributed in two groups manually by writing specific numbers that will be concealed in sequentially numbered, opaque sealed envelopes. The envelopes will be opened by an attending nurse not involved in the study just before the procedure. The incision will be given by the attending general surgery resident who will perform the inguinal hernia repair. The assessment of pain and data collection, data analysis will be done by principle investigator who is blinded to procedure. Thus, the patients and investigating and analyzing personal will be blinded to the procedure.
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Group 1: Scalpel
    Arm Type
    Active Comparator
    Arm Description
    Skin Incision for inguinal hernia repair will be given by Stainless steel blade no.10. Open Mesh Hernioplasty
    Arm Title
    Group 2 : Electrocautery
    Arm Type
    Experimental
    Arm Description
    Open Mesh Hernioplasty Skin Incision for inguinal hernia repair will be given by following: Cautery machine: Erbe VIO 300 S Cut setting: Cut:30 Coagulate:30 Cautery tip (tip pointed) Mode: Monopolar
    Intervention Type
    Procedure
    Intervention Name(s)
    Open Mesh Hernioplasty
    Intervention Description
    Steps of surgery: Injection Ceftriaxone 50 mg/kg iv stat dose will be given pre-operatively Incision: Incision given over medial 3/5 and 2.5 cms above and parallel to inguinal ligament extending from pubic tubercle upto 1 cm lateral to mid point of inguinal ligament. bleeding controlled by forcep coagulation. Cut the subcutaneous tissues,external oblique aponeurosis opened in layers Nerve Iliohypogastric & ilioinguinal will be preserved (by taking aside from the field) Intra-operative Injection Tramadol(50 mg) and ondansetron(4 mg) iv stat dose given Sac ligated with Polygalactin 2-0 suture. Lichtenstein method of repair Mesh type: large pore polypropylene mesh Mesh size: 3 x 6 inches(7.5 x 15 cms) Mesh Fixation: polypropylene 2-0 External oblique closure Skin closure: Ethilon 2 - 0 suture
    Primary Outcome Measure Information:
    Title
    To Compare the incidence of post-operative pain between two groups.
    Description
    For assessment of pain; visual analog scale will be used in every patients.
    Time Frame
    Assessment of Pain will be done • immediately after surgery, 30 minutes , 1 hour • Day 1 to day 5 (Telephone conversation)
    Secondary Outcome Measure Information:
    Title
    To compare the post-operative analgesic dose requirement between the two groups.
    Description
    For assessment of analgesic dose requirement; will be asked using the telephone conversation.
    Time Frame
    Day 1 to Day 5
    Title
    To Compare the incidence of other complications like SSI, Hematoma, Seroma and Urinary retention between the two groups.
    Description
    For assessment of other post-operative complications ; patient will be followed up in OPD after telephone conversation.
    Time Frame
    Day 1 to Day 5

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients ≥ 18 years old who are operated with the diagnosis of inguinal hernia. Exclusion Criteria: Patients with recurrent inguinal hernia Patients presenting with incarcerated, irreducible and strangulated hernia Bilateral Inguinal Hernia Patient taking steroids Patient with contraindication to NSAIDs such as CKD, Drug hypersensitivity etc Patients who do not give written consent
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Sanjeeb kr Jha, MBBS
    Phone
    +977-9851127004
    Email
    dr.sanjeeb.jha@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Bikal Ghimire, MCh
    Phone
    +977-9851095679
    Email
    bikalghimire@gmail.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Yogendra Pd Singh, MBBS,MS
    Organizational Affiliation
    Tribhuvan University Teaching Hospital, Institute Of Medicine.
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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