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Effect of Intraperitoneal Infiltration of Bupivacaine and Fentanyl Combination on the Pain Control after Diagnostic Gynecologic Laparoscopy

Effect of Intraperitoneal Infiltration of Bupivacaine and Fentanyl Combination on the Pain Control after Diagnostic Gynecologic Laparoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201212267013N4
Enrollment
100
Registered
2013-01-06
Start date
2013-01-20
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 due to diagnostic laparoscopy. Female infertility

Interventions

Intervention 1: In the study group(n=50) 40mL of 0. 25% bupivacaine with 100 µg fentanyl is infiltrated intraperitonealy at the end of operation. Intervention 2: In the placebo group(n=50) 40 ml norma
Treatment - Drugs
In the study group(n=50) 40mL of 0. 25% bupivacaine with 100 µg fentanyl is infiltrated intraperitonealy at the end of operation.
In the placebo group(n=50) 40 ml normal saline is infiltrated intraperitonealy at the end of operation.

Sponsors

Vice Chancellor for Research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients scheduled for diagnostic gynecologic laparoscopy; patients aged 18–40 yr; patients with ASA class I or II. Exclusion criteria: Patients with a history of allergy to local anesthetics; patients with a history of systemic disease or psychological disorders; patients with a history of chronic pain syndrome; Patients with a history of NSAIDS or any other analgesic consumption.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: PACU, every 1 hour until 4 hours and then every 4 hours until 24 hours after operation. Method of measurement: Visual analogue scale (VAS) from 0 (without pain) to 10 (severe and intolerable pain).

Secondary

MeasureTime frame
Dose of analgesic requirements. Timepoint: PACU, every 1 h until 4 h and then every 4 h until 24 h after operation. Method of measurement: Injection number and injection dose in mg.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Simin Atashkhoyi

Tabriz University of Medical Sciences

siminatashkhoii@yahoo.comsatashkhoyi@gmail.com+98 41 1553 9161

Outcome results

None listed

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