Skip to content

Efficacy of diclofenac suppository shoulder pain and scapula after laparoscopic cholecystectomy

Efficacy of diclofenac suppository shoulder pain and scapula after laparoscopic cholecystectomy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015102013865N2
Enrollment
100
Registered
2016-06-15
Start date
2015-01-21
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

Laparoscopy. Postprocedural disorders of genitourinary system, not elsewhere classified

Interventions

Intervention 1: Intervention group diclofenac suppository (100 mg- Iran Najo Pharmaceutical ) after induction of anesthesia and before rectal surgery may be recommended. Intervention 2: Diclofenac sup
Treatment - Drugs
Intervention group diclofenac suppository (100 mg- Iran Najo Pharmaceutical ) after induction of anesthesia and before rectal surgery may be recommended.
Diclofenac suppository is not recommended for patients in the control group

Sponsors

Deputy of Reaserch and Technology of Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: all patients who are candidates for laparoscopic cholecystectomy; pleased to participate in the study Exclusion criteria: patients with a history of sleeping pills or drugs within 24 hours before surgery, the patients who are contraindicated diclofenac or analgesic, patients who are drug addicts, patients who are allergic to NSAID drugs and surgical patients they changed to open surgery

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Paine. Timepoint: During the first 3 hours after surgery, 6 hours and 12 hours after surgery. Method of measurement: Using the NRS scale & record severe pain intensity.

Secondary

MeasureTime frame
Nausea. Timepoint: 24 hours after surgery. Method of measurement: Question of the patient.;Vomiting. Timepoint: 24 hours after surgery. Method of measurement: Question of the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Alireza Kamel

Babol University of Medical Sciences

bcrdc90@yahoo.com+98 11 3219 7667

Outcome results

None listed

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