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Comparison of transdermal diclofenac patch with IM diclofenac for post operative analgesia in lap chole

Compare the efficacy of transdermal diclofenac patch with intramuscular diclofenac for post op analgesia in laparoscopic cholecystectomy:Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058555
Enrollment
60
Registered
2023-10-12
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: INJECTION DICLOFENAC 75 MG: GROUP B INJECTION DICLOFENAC 75 mg 30 minutes before extubation stat dose by intramuscular route.Total duration for intervention is for one year Control Inte

Sponsors

Rohilkhand medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American society of Anaesthesiologist (ASA) grade I or II. Age group Between 18-60 yrs of either sex

Exclusion criteria

Exclusion criteria: Pregnant females. Patients with co-morbid diseases like diabetes, hypertension, TB, HIV, neurological,psychiatric or neuro-vascular disorders. Patients with history of asthma,urticaria and hypersensitivity to any component of diclofenac patch or injection. Patients with gastrointestinal tract related problems(gastritis, ulcers, bleeding & perforation). Patients with skin diseases (eczema, fungal infection, inflammation, burn wound). Patients with history of alcohol abuse, blood (porphyria, bleeding or clotting disorders) and vascular disorder.

Design outcomes

Primary

MeasureTime frame
To compare the analgesic effect between transdermal patch of diclofenac and intramuscular diclofenac. To document adverse effects. To assess requirement of rescue analgesia. To compare VAS and QoR-15 score for one year Timepoint: To compare the analgesic effect between transdermal patch of diclofenac and intramuscular diclofenac at 2,4,6,8,10,12,24 hours. To document adverse effects at 2,4,6,8,10,12,24 hours. To assess requirement of rescue analgesia at 2,4,6,8,10,12,24 hours. To compare VAS score at 2,4,6,8,10,12,24 hours and QoR-15 score after 24 hours. Total Duration for one year

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Sarfaraz Ahmad

Rohilkhand medical college and hospital

umapurohit58@gmail.com9927004515

Outcome results

None listed

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