- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05107986
Laparoscopy in Complicated Groin Hernia
October 23, 2021 updated by: Bhawani Khanal, B.P. Koirala Institute of Health Sciences
Outcomes of Laparoscopic Repair in Complicated Groin Hernia: a Single Institutional Based Cohort Study in Nepal
This study assessed the outcomes of laparoscopic repair in complicated groin hernia.
Laparoscopic approach in cases of complicated groin hernia can achieve desirable patient outcomes without major complications, provided good patient selection and expertise.
This study provides an insight to the outcomes from the procedure in low resource setting of Nepal.
Study Overview
Study Type
Observational
Enrollment (Actual)
22
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Province 1
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Dharān Bāzār, Province 1, Nepal, 56700
- BP Koirala Institute of Health Sciences
-
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients with diagnosis of complicated groin hernia
Description
Inclusion Criteria:
- Patients with age greater than 18 years with diagnosis of complicated groin hernia
Exclusion Criteria:
- Patients with features of peritonitis, history of previous abdominal surgery and those unfit for general anesthesia
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Patients diagnosed with complicated groin hernia
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All patients of cohort underwent laparoscopic repair.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
intraoperative complications
Time Frame: during surgical procedure
|
1. Bleeding (epigastric / testicular vessels) 2. Bowel injury 3. Peritoneal tear
|
during surgical procedure
|
|
Postoperative complications
Time Frame: upto 6 months post operatively
|
1. Seroma 2.Urinary Retention 3. Wound infection
|
upto 6 months post operatively
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2017
Primary Completion (Actual)
May 20, 2018
Study Completion (Actual)
September 30, 2018
Study Registration Dates
First Submitted
October 7, 2021
First Submitted That Met QC Criteria
October 23, 2021
First Posted (Actual)
November 4, 2021
Study Record Updates
Last Update Posted (Actual)
November 4, 2021
Last Update Submitted That Met QC Criteria
October 23, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRC/1217/018
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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