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efficacy of Location of drains in abdominal pain after laparoscopic surgery for obesity.

Clinical trial examining the effect of the location of drains in abdominal pain after laparoscopy gastric bypass surgery Roux en y procedure in morbid obese

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201202198588N3
Enrollment
50
Registered
2012-07-25
Start date
2011-05-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

post operative abdominal pain. Other and unspecified abdominal pain

Interventions

Prevention
The drain will be extracted from the right side of the patients.
Intervention 1: The drain will be extracted from the right side of the patients. Intervention 2: The drain will be extracted from the left side of the patients.
The drain will be extracted from the left side of the patients.

Sponsors

Teran University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 64 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Morbid obese patients with BMI over 40 or over 35 with one obese comorbidity such as metabolic disease, diabetes, HTN, HLP, Hyperbaric metabolic states;who are undergoing obesity surgery. Exclusion criteria: Patients who underwent laparoscopic surgery who converte to open?Patients with activated drain for any reason(bleeding or Lake);The patients that forced us to maintain the drain for them over 24 hours.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Abdominal Pain. Timepoint: 24 hours after intervention, one week after internetion,1 month after intervention. Method of measurement: Visual Analogue Scale (VAS).

Secondary

MeasureTime frame
Drain site infection. Timepoint: one week after intervention. Method of measurement: Clinical examination.;Small bowel herniation through drain extraction site. Timepoint: 24 hours after intervention, 1 week after intervention, 1 month after intervention. Method of measurement: Clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Mohammad eidy

Minimally Invasive Surgery Research Center, Tehran University of Medical Sciences.

m_eidy1356@yahoo.com+98 21 6655 5447

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026