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comparison of pain killer patch with pain relief procedure for inguinal surgeries

An evaluation of transdermal Buprenorphine, Fentanyl patches and regional blocks on analgesic effect and quality of recovery following inguinal hernia surgery - a randomized study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047271
Enrollment
150
Registered
2022-11-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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: Transdermal fentanyl patch: Transdermal Fentanyl patch applied 12 hours prior surgery and Pain will be assessed by NRS SCORE AT 4,8,12,24,48 hours after surgery Intervention2: Transder

Sponsors

All India Institute of Medical Sciences, Bibinagar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA 1 & 2 2. Inguinal hernia surgeries

Exclusion criteria

Exclusion criteria: 1. known allergy to the test drug 2. hepatic disease, renal disease 3. chronic alcoholic 4. suffering from any other chronic pain syndrome 5. patients taking opioids, NSAIDS, or any pain medication for more than 3 months, on antiepileptics or antidepressants

Design outcomes

Secondary

MeasureTime frame
QoR score Time for rescue analgesiaTimepoint: POD1, POD2, POD3, POD4, POD5—

Primary

MeasureTime frame
NRS ScoreTimepoint: at the end of surgery, 1 hour, 2 hours, 6 hours, 12 hours, 24 hours, 48 hours, 72 hours—

Countries

India

Contacts

Public ContactDr CH Rama Krishna Prasad

All India Institute of Medical Sciences, Bibinagar

ramakrishna.chikkala19@gmail.com

Outcome results

None listed

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