CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 94 enrolled
Drug / intervention
Pneumoperitoneum Pressureprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03179111
NCT03179111N/ACompleted
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Evaluation of Low Pressure Pneumoperitoneum in Bariatric Surgery: A Prospective Randomized Study

Universiti Putra Malaysia·interventional·Posted Jun 7, 2017·Updated May 7, 2018

In Brief

A clinical study evaluating Pneumoperitoneum Pressure for Surgical View and 2 related conditions. Completed, enrolled 94 participants across 1 site.

Detailed Summary

This is a prospective study whereby it involves patients who are planned for bariatric surgery. In the bariatric surgery procedure, pneumoperitoneum pressure will be the experimental aspect in this study. The pneumoperitoneum pressure will be adjusted to either 8-10 mmHg of low pressure or to 12-15mmHg of standard pressure.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSurgical View, Shoulder Tip Pain, Abdominal Pain
CountriesMalaysia
Collaborators--

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedJun 7, 2017
Enrollment StartAug 30, 2017
Primary CompletionMay 4, 2018
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 9.1 years ago

Interventions

Pneumoperitoneum Pressureprocedure

There will be two arms in this study. The participants recruited for this study are those who have been screened and planned for elective bariatric surgery.The pneumoperitoneum pressure will be adjusted to either 8-10mmHg or 12-15mmHg until a clear operating field is obtained by the surgeon. Low pneumoperitoneum pressure has been expected to give a clearer and better surgical view than standard pneumoperitoneum pressure. Participants under the low pressure group are expected to have lesser pain score on abdominal pain and shoulder tip pain as compared to participants in the standard pressure group.