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Comparing the pain relief effect of two types of pain killers in patients of hernia surgery

Comparative study of analgesic efficacy and tolerability of oral tapentadol-paracetamol combination vs. oral tramadol-paracetamol combination for postoperative pain relief in patients undergoing hernia surgery - None

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/08/007217
Enrollment
120
Registered
2016-08-23
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: null- Male patients 18 to 70 years Inguinal Hernia Surgery ASA 1 and 2 status Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Oral Tapentadol and paracetamol: In patients following hernia surgery, when the level of subarachnoid block will recede to T10 then patients will receive combination of oral tapentadol

Sponsors

Government Medical College and Hospital
Lead Sponsor
Anaesthesia and Intensive care
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Under going inguinal hernia surgery ASA status I and II

Exclusion criteria

Exclusion criteria: 1. ASA status > III 2. Major co-existing medical illness (especially severe asthma/COPD, epilepsy, uncontrolled hypertension or diabetes, liver or renal disease) 3. Patients with paralytic ileus 4. Patients on tricyclic antidepressants, anticonvulsants, Mono amino oxidase inhibitors, antipsychotics or serotonin-norepinephrine reuptake inhibitors (i.e. within 30 days) 5. Known hypersensitivity to any of the study medications.

Design outcomes

Primary

MeasureTime frame
Pain at rest and on movement measured by visual analog scale (VAS)Timepoint: During the postoperative period at intervals of 0 hour (when the first dose of the combination is administered, i.e., when the block level recedes to T10), 2, 4, 8, 12, and 24 h

Secondary

MeasureTime frame
Haemodynamics,Patient Satisfaction Scale , rescue analgesics, adverse effectsTimepoint: During the postoperative period at intervals of 0 hour (when the first dose of the combination is administered, i.e., when the block level recedes to T10), 2, 4, 8, 12, and 24 h

Countries

India

Contacts

Public ContactVanita Ahuja

Department of Anaesthesia and Intensive care Government Medical College and Hospital sector 32

vanitaanupam@yahoo.co.in

Outcome results

None listed

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