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Effect of site of catheter for bupivacain administration in laparotomy wound on postoperative pain

Evaluation of effect of site of catheter for bupivacain administration in midline laparotomy on postoperative pain in Shariati hospital patients in 2011-2012

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138810142982N1
Enrollment
60
Registered
2011-11-04
Start date
2011-03-21
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

Pain management after laparotomy.

Interventions

Intervention 1: In group "Catheter between fascia", two infant feeding tubes (6 Fr) - with added holes - are place between rectus muscle and posterior fascia. 20 cc of bupivacain 0.25% are administere
Treatment - Surgery
In group "Catheter between fascia", two infant feeding tubes (6 Fr) - with added holes - are place between rectus muscle and posterior fascia. 20 cc of bupivacain 0.25% are administered via each cathe
In group "Catheter on the fascia", after fascia closure, two infant feeding tubes (6 Fr) - with added holes - are placed over the fascia in subcutaneous space. 20 cc of bupivacain 0.25% are administer

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients undergoing midline laparotomy for elective surgeries and sign informed consent for participating in the study Exclusion Criteria: substance abuse, no appropriate verbal communication, simultaneous other incisions, critically ill or unstable patients, being unconscious or intubated in postoperative period

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Total postoperative narcotic consumption. Timepoint: Untill 72 hours based on PCA device. Method of measurement: Patient controlled analgesia device.

Secondary

MeasureTime frame
Postoperative nausea and vomitting. Timepoint: daily till 48 hours after surgery. Method of measurement: History taking and clinical records.;Postoperative Cardiavascular complications. Timepoint: daily till 48 hours after surgery. Method of measurement: based on medical reocords.;Postoperative pulmonary complications. Timepoint: daily till 48 hours after surgery. Method of measurement: based on medical reocords.;Wound infection. Timepoint: daily till 5 days after surgery. Method of measurement: Physical examination.;Hospital stay. Timepoint: At the time of discharge. Method of measurement: based on medical reocords.;Postoperative pain. Timepoint: 12 hours intervals for 3 days. Method of measurement: Visual analogue scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZhamak Khorgami

Tehran University of Medical Sciences - Shariati Hospital

khorgami@gmail.com+98 21 8490 2450

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 24, 2026