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Randomised Controlled Trial on Pre-peritoneal Drainage After Totally Extra-peritoneal Hernioplasty for Inguinal Hernia

Primary Purpose

Hernia, Inguinal

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
preperitoneal suction drainage
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hernia, Inguinal focused on measuring Hernia, Inguinal, Extraperitoneal Hernioplasty, Drain, Mesh Repair, Laparoscopic

Eligibility Criteria

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

Inclusion Criteria:

  • Age above 18 and below 80
  • Male or female patients
  • Unilateral inguinal hernia
  • First occurrence hernia
  • Consent to laparoscopic hernioplasty for inguinal hernia

Exclusion Criteria:

  • Inguino-scrotal hernia
  • Recurrent inguinal hernia
  • Incarcerated hernia
  • Bilateral inguinal hernia
  • Bleeding tendency
  • On anti-platelet agent or anti-coagulant
  • Co-morbidies
  • Decline or not consent to surgery

Sites / Locations

  • Department of Surgery, The University of Hong Kong - Shenzhen HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Drain

No-drain

Arm Description

preperitoneal suction drainage after laparoscopic totally extra-peritoneal hernioplasty for inguinal hernia

No drainage after laparoscopic totally extra-peritoneal hernioplasty for inguinal hernia

Outcomes

Primary Outcome Measures

Seroma formation after TEP hernioplasty
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
Seroma formation after TEP hernioplasty
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
Seroma formation after TEP hernioplasty
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
Seroma formation after TEP hernioplasty
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
Seroma formation after TEP hernioplasty
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
Seroma formation after TEP hernioplasty
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP

Secondary Outcome Measures

Post-operative pain after TEP hernioplasty
Post-operative pain after TEP hernioplasty will be assessed by self-evaluated VAS questionnaire during initial 7 days after operation. Then will be asked by independent assessor upon follow-up
Analgesic used after after TEP hernioplasty
Number of analgesic used after after TEP hernioplasty will be assessed by self-evaluated questionnaire during initial 7 days after operation. Then will be asked by independent assessor upon follow-up
Chronic discomfort after TEP hernioplasty
Chronic discomfort after TEP hernioplasty will be asked by independent assessor upon follow-up
Hernia recurrence after TEP hernioplasty
Hernia recurrence after TEP hernioplasty will be assessed by independent assessor upon follow-up
Patient satisfaction after TEP hernioplasty
Patient satisfaction after TEP hernioplasty will be asked by independent assessor upon follow-up

Full Information

First Posted
May 3, 2016
Last Updated
May 8, 2016
Sponsor
The University of Hong Kong
Collaborators
The University of Hong Kong-Shenzhen Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02762747
Brief Title
Randomised Controlled Trial on Pre-peritoneal Drainage After Totally Extra-peritoneal Hernioplasty for Inguinal Hernia
Official Title
Pre-peritoneal Drainage Versus No Drainage After Totally Extra-peritoneal Hernioplasty for Inguinal Hernia - a Randomised Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Unknown status
Study Start Date
May 2016 (undefined)
Primary Completion Date
May 2018 (Anticipated)
Study Completion Date
August 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
Collaborators
The University of Hong Kong-Shenzhen Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a RCT on drain versus no drain after laparoscopic totally extra-peritoneal hernioplasty. We will assess the difference in seroma formation after surgery in 2 two groups by an independent assessor clinically and radiologist to document the size of seroma after surgery. Other secondary outcomes will be measured including post-operative pain, discomfort, analgesic used, patient satisfaction, recurrence of hernia, wound infection, etc.
Detailed Description
Inguinal hernia is a common disease and causes significant morbidity if left untreated. With the advances of laparoscopic approach of extra-peritoneal hernioplasty, it significantly reduces the post-operative pain and lead to a better quality of life with higher acceptance to patients.However, similar to traditional Litchenstein approach, post operative seroma formation is still a common problem encountered after surgery. Numerous method has been described to reduce chance of seroma formation, however, none was proven to be effective except pre-peritoneal drainage. There are currently 2 large retrospective non-randomized cohort study to evaluate the effectiveness of preperitoneal drainage available for reference. We therefore study the feasibility and efficacy of preperitoneal drainage with large scale randomized trial. Patient fulfill inclusion criteria and consent to surgery and study will be recruited. A standardized pre-peritoneal dissection and mesh placement will be adopted. Immediately before deflation of pre-peritoneal space, randomization will be performed by calling research assistant for study group using computer generated code. Drain will be placed for 23 hours after operation and ultrasonography will be performed immediately after removal of drain. USG will be repeated at post-operative 1 week, 1 month, 3 months, 6 months and 1 year after surgery. For non-drain group, a fake drain will be attach to the skin of the wound to achieve double blinding to patients and assessors. In addition to seroma, patient demographics and secondary outcome including post-operative pain score, discomfort, foreign body sensation, patient satisfaction, infection, recurrence, etc will be studied.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hernia, Inguinal
Keywords
Hernia, Inguinal, Extraperitoneal Hernioplasty, Drain, Mesh Repair, Laparoscopic

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Drain
Arm Type
Experimental
Arm Description
preperitoneal suction drainage after laparoscopic totally extra-peritoneal hernioplasty for inguinal hernia
Arm Title
No-drain
Arm Type
No Intervention
Arm Description
No drainage after laparoscopic totally extra-peritoneal hernioplasty for inguinal hernia
Intervention Type
Procedure
Intervention Name(s)
preperitoneal suction drainage
Intervention Description
preperitoneal suction drainage after laparoscopic totally extra-peritoneal hernioplasty for inguinal hernia
Primary Outcome Measure Information:
Title
Seroma formation after TEP hernioplasty
Description
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
Time Frame
post-operative day 1
Title
Seroma formation after TEP hernioplasty
Description
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
Time Frame
post-operative day 7
Title
Seroma formation after TEP hernioplasty
Description
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
Time Frame
post-operative 1 month
Title
Seroma formation after TEP hernioplasty
Description
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
Time Frame
post-operative 3 month
Title
Seroma formation after TEP hernioplasty
Description
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
Time Frame
post-operative 6 month
Title
Seroma formation after TEP hernioplasty
Description
Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
Time Frame
post-operative 1 year
Secondary Outcome Measure Information:
Title
Post-operative pain after TEP hernioplasty
Description
Post-operative pain after TEP hernioplasty will be assessed by self-evaluated VAS questionnaire during initial 7 days after operation. Then will be asked by independent assessor upon follow-up
Time Frame
post-operative day 1 to day 7, 1 month, 3 month, 6 month, 1 year
Title
Analgesic used after after TEP hernioplasty
Description
Number of analgesic used after after TEP hernioplasty will be assessed by self-evaluated questionnaire during initial 7 days after operation. Then will be asked by independent assessor upon follow-up
Time Frame
post-operative day 1 to day 7, 1 month, 3 month, 6 month, 1 year
Title
Chronic discomfort after TEP hernioplasty
Description
Chronic discomfort after TEP hernioplasty will be asked by independent assessor upon follow-up
Time Frame
post-operative 1 month, 3 month, 6 month, 1 year
Title
Hernia recurrence after TEP hernioplasty
Description
Hernia recurrence after TEP hernioplasty will be assessed by independent assessor upon follow-up
Time Frame
post-operative 1 month, 3 month, 6 month, 1 year
Title
Patient satisfaction after TEP hernioplasty
Description
Patient satisfaction after TEP hernioplasty will be asked by independent assessor upon follow-up
Time Frame
post-operative 1 month, 3 month, 6 month, 1 year

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: Age above 18 and below 80 Male or female patients Unilateral inguinal hernia First occurrence hernia Consent to laparoscopic hernioplasty for inguinal hernia Exclusion Criteria: Inguino-scrotal hernia Recurrent inguinal hernia Incarcerated hernia Bilateral inguinal hernia Bleeding tendency On anti-platelet agent or anti-coagulant Co-morbidies Decline or not consent to surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joe KM Fan, MBBS,MS,FRCS
Phone
+86-18307555114
Email
drjoefan@hku.hk
First Name & Middle Initial & Last Name or Official Title & Degree
WL Law, MBBS,MS,FRCS
Phone
+852-22554763
Email
lawwl@hku.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joe KM Fan, MBBS,MS,FRCS
Organizational Affiliation
The University of Hong Kong
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Surgery, The University of Hong Kong - Shenzhen Hospital
City
Shenzhen
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joe KM Fan, MBBS,MS,FRCS
Phone
+86-18307555114
Email
drjoefan@hku.hk
First Name & Middle Initial & Last Name & Degree
WL Law, MBBS MS FRCS
First Name & Middle Initial & Last Name & Degree
Dominic CC Foo, MBBS FRCS
First Name & Middle Initial & Last Name & Degree
JW Liu
First Name & Middle Initial & Last Name & Degree
XF Yang
First Name & Middle Initial & Last Name & Degree
KJ Chen

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
19542859
Citation
Ismail M, Garg M, Rajagopal M, Garg P. Impact of closed-suction drain in preperitoneal space on the incidence of seroma formation after laparoscopic total extraperitoneal inguinal hernia repair. Surg Laparosc Endosc Percutan Tech. 2009 Jun;19(3):263-6. doi: 10.1097/SLE.0b013e3181a4d0e1.
Results Reference
result
PubMed Identifier
25238803
Citation
Gao D, Wei S, Zhai C, Chen J, Li M, Gu C, Wu H. Clinical research of preperitoneal drainage after endoscopic totally extraperitoneal inguinal hernia repair. Hernia. 2015 Oct;19(5):789-94. doi: 10.1007/s10029-014-1310-0. Epub 2014 Sep 20.
Results Reference
result

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Randomised Controlled Trial on Pre-peritoneal Drainage After Totally Extra-peritoneal Hernioplasty for Inguinal Hernia

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