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Comparing the pain relief by diclofenac given as intravenous or skin patch to patients undergoing middle ear surgery

An observational study to compare the effect of intravenous versus transdermal diclofenac on post operative pain in middle ear surgeries under General Anesthesia - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104394
Enrollment
150
Registered
2026-02-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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: Intravenous diclofenac: Patients in group I will be given intravenous diclofenac 8 hourly postoperatively Control Intervention1: Transdermal diclofenac patch: Patients in group T will b

Sponsors

Peoples Hospital Bhopal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of age between 18-45 years of both female and male gving informed consent

Exclusion criteria

Exclusion criteria: 1)Patients not giving informed consent 2)Patients with history of hypersensitivity with diclofenac 3)ASA grade more than II 4)History of peptic ulcer disease 5)Known case or history of renal dysfunction

Design outcomes

Primary

MeasureTime frame
Pain after middle ear surgeryTimepoint: 48 hours—

Secondary

MeasureTime frame
Haemodynamic parametersTimepoint: 48 hours—

Countries

India

Contacts

Public ContactDr Mahima Batra

PCMS and RC Bhopal

drmahimabatra@gmail.com9752075418

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026