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Preemptive morphine suppository for postoperative pain relief after laparoscopic cholecystectomy

Preemptive morphine suppository for postoperative pain relief after laparoscopic cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015010620588N1
Enrollment
70
Registered
2015-07-11
Start date
2014-07-01
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

Postcholecystectomy syndrome. Disorders of gallbladder, biliary tract and pancreas

Interventions

Intervention 1: The patients in the intervention group (MS group – morphine suppository group) will receive 10 milligram morphine rectal suppository) just before induction of anesthesia. Intervention
Prevention
Treatment - Drugs
The patients in the intervention group (MS group – morphine suppository group) will receive 10 milligram morphine rectal suppository) just before induction of anesthesia.
The patients in the control group will receive suppository schiafs similar to morphine suppository schiafs in appearance just bofore the induction of anesthesia.

Sponsors

Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: ASA physical status I-II? candidates for elective laparoscopic cholecystectomy under general anesthesia; age span from 18 to 65 years; body mass index (BMI) less than 30; lack of sensitivity to morphine and or similar compounds; lack of addiction to opioids; and no renal liver failure. exclusion criteria:ASA>2; Any event that leads to changing the Anesthesia or surgery technique.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: On arrival to recovery room, and then 30, 60, minutes and 2, 4, 8, 16, 24 hours after that. Method of measurement: VAS SCORE.

Secondary

MeasureTime frame
Decreasing of the total dose of analgesics. Timepoint: From 30 minutes after recovery to 24 hours after surgery. Method of measurement: measurement of total analgesic drugs used.;Hemodynamic stability. Timepoint: From 30 minutes after recovery to 24 hours after surgery. Method of measurement: By pulse oxymetery; non invasive blood pressure monitoring;.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDarioush Moradi Farsani

Isfahan University of Medical Science

dmoradi@med.mui.ac.ir-drdmoradi@gmail.com+98 313625555

Outcome results

None listed

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