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UnknownNCT04960267

Use of Pre-peritoneal Drainage in rTAPP - a Comparative Study

Use of Pre-peritoneal Drainage in rTAPP - a Comparative Study With Laparoscopic TEP

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
The University of Hong Kong · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The safety and efficacy of pre-peritoneal drain after TEP has been validated in our previous studies - which can effectively reduce seroma formation post-operatively and safe in clinical use. We shall extend the indication of pre-peritoneal drainage after robotic TAPP, results will be compared with our retrospective cohort from previous studies.

Detailed description

The safety and efficacy of pre-peritoneal drain after TEP has been validated in our previous studies - which can effectively reduce seroma formation post-operatively and safe in clinical use. We shall extend the indication of pre-peritoneal drainage after robotic TAPP, results will be compared with our retrospective cohort from previous studies. Criteria of enrolling into trial is same as our previous experiment: aged 18-80, unilateral, first occurrence, reducible, non-inguino-scrotal inguinal hernia fit for GA for minimally invasive hernia repair. Routine robotic TAPP performed in standardized manner and pre-peritoneal drains are placed for drainage of 23 hours post-operatively. Drain output, pain scores, status of seroma formation (clinical, USG detected), post-operative recovery and recurrence will be monitored and compared.

Conditions

Interventions

TypeNameDescription
DEVICEUse of pre-peritoneal drainage after rTAPPUse of pre-peritoneal drainage after rTAPP

Timeline

Start date
2021-02-01
Primary completion
2021-09-01
Completion
2021-11-01
First posted
2021-07-13
Last updated
2021-07-13

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04960267. Inclusion in this directory is not an endorsement.

Use of Pre-peritoneal Drainage in rTAPP - a Comparative Study (NCT04960267) · Clinical Trials Directory