Clinical Trials Directory

Trials / Completed

CompletedNCT03563092

Closed Suction Drain vs no Drain on Symptomatic Seroma Formation After Laparoscopic Inguinal Hernia Repair

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
GEM Hospital & Research Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The current study aims to determine whether a use of closed suction drain following laparoscopic inguinal hernia surgery performed for an inguinoscrotal variety can decrease the incidence of symptomatic seroma formation requiring interventions and thus, prevent postoperative morbidity.

Detailed description

Patients with laparoscopic inguinal repair, TEP as well as TAPP approach, which matches the inclusion criteria will be randomized intraoperatively, based on a complete assessment of eligibility, just before the mesh placement. Patients recruited in closed suction drain arm will receive suction drain(14 French sizes) in preperitoneal space via a separate incision. The patients without drain arm, the regular postoperative course will be followed. The drain will be removed once the output falls below 50 ml per day. Both groups will be followed up until three months post-surgery. Clinical suspicion of seroma in symptomatic patients will be confirmed by ultrasound. Seroma will be managed conservatively till three weeks in the post-op period.

Conditions

Interventions

TypeNameDescription
PROCEDURELaparoscopic Inguinal Hernia (TEP/TAPP) SurgeryStandardized minimally invasive approach to inguinal hernia repair

Timeline

Start date
2018-08-01
Primary completion
2019-09-15
Completion
2019-11-30
First posted
2018-06-20
Last updated
2020-10-14

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT03563092. Inclusion in this directory is not an endorsement.