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Preemptive Analgesia with Oral Tapentadol

Effect of Preemptive Analgesia with Tapentadol on Post Operative Analgesic requirements in patients Undergoing Unilateral inguinal Hernia Surgery under Spinal Anaesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/03/018130
Enrollment
60
Registered
2019-03-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K409- Unilateral inguinal hernia, without obstruction or gangrene

Interventions

Intervention1: Oral Tapentadol 100 mg: Tapentadol 100mg tablet given orally 30 minutes before the surgery. Control Intervention1: placebo capsules: placebo capsules administered 30 minutes before surg

Sponsors

Vinayaga Missions Medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy adults undergoing Unilateral Inguinal Hernia surgery ASA physical status 1 and 2

Exclusion criteria

Exclusion criteria: Presence of systemic disorders Patient not suitable for spinal anesthesia Patients on opioid use BMI more than 35 ASA physical status 3 and 4 Pregnant women history of allergy to study drugs

Design outcomes

Primary

MeasureTime frame
Post operative Analgesic requirementTimepoint: At immediate post operative period and at hourly interval till 24 hours.—

Secondary

MeasureTime frame
Incidence of adverse effects like nausea, vomiting, drowsiness, prutitusTimepoint: During surgery and at 1,2,3,4,5,6 hours and every 2 hours thereafter—

Countries

India

Contacts

Public Contactk Vinith Kumar

Vinayaka missions medical college

vinithkumar1403@gmail.com9790243751

Outcome results

None listed

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