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COMPARATIVE STUDY OF TRANSDERMAL DICLOFENAC PATCH AND INJECTION DICLOFENAC IN PATIENTS WITH INGUINAL HERNIA SURGERY FOR POSTOPERATIVE PAIN RELIEF.

COMPARATIVE STUDY OF TRANSDERMAL DICLOFENAC PATCH VERSUS IM INJECTION DICLOFENAC IN PATIENTS WITH INGUINAL HERNIA SURGERY:POST OPERATIVE PAIN RELIEF.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046425
Enrollment
100
Registered
2022-10-12
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: - Health Condition 2: M959- Acquired deformity of musculoskeletal system, unspecified Health Condition 3: M959- Acquired deformity of musculoskeletal system, unspecified

Interventions

Intervention1: diclofenac patch 100 mg: diclofenac patch 100 mg in group DP will be applied just after induction of spinal anesthesia in on contralateral side . Control Intervention1: diclofenac intr

Sponsors

DR AFREEN SHAMSUDDIN BOAT
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient undergoing inguinal hernia correction surgeries who are hemodynamically stable, with all routine investigations within normal limits without any other co morbidities.

Exclusion criteria

Exclusion criteria: Patients with ASA physical status III or more. Patients contraindicated for spinal anesthesia. Patients with co- morbidities like diabetes, hypertension, neurological, psychiatric or neurovascular disorders. Patients with drug allergies. Patient refusal.

Design outcomes

Primary

MeasureTime frame
VAS SCORE 0-1Timepoint: 12 hours post operative.—

Secondary

MeasureTime frame
VAS SCORE 1-2Timepoint: at 24 hours post operative.—

Countries

India

Contacts

Public ContactDR AFREEN SHAMSUDDIN BOAT

DR DY PATIL MEDICAL COLLEGE , PIMPRI , PUNE.

drbhavinishah71@gmail.com9850829994

Outcome results

None listed

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