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Comparison of efficiency in reliving pain after surgery between two drugs clonidine and pregabalin when given orally prior to surgery

Comparison Of Pre-operative Administration Of Oral Pregabalin Versus Clonidine For Immediate Post Operative Pain In Infra-umbilical Surgeries Under Sub-Arachnoid Block.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/10/028287
Enrollment
90
Registered
2020-10-08
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: 8- Other Procedures

Interventions

Intervention1: Subarachnoid block with hyperbaric bupivacaine in infra umbilical surgeries alongwith preoperative oral pregabalin.: Tablet pregabalin(150 mg), will be given to the patients with a sip

Sponsors

Office of PrincipalMidnapore Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Cases with ASA grade I and II. Age group between 18-65 years. Cases with height between 150-180cms. Patients willing to give written consent. Patients with body weight 50-70kg. Cases undergoing infra-umbilical surgeries performed under subarachnoid block.

Exclusion criteria

Exclusion criteria: Cases which has contraindication to spinal anaesthesia. Cases with ASA grade III and above. Patients undergoing upper abdominal surgeries. Pregnant and lactating patients. Patients with psychiatric disorders. Cases with history of allergy or hypersensitivity to study drugs. Cases with any neuropathy or neurological disorder. Patients with any ongoing therapies with sustained release opioids. Any cardio-respiratory disorder. Any hepato-renal disorders. Immuno-compromised patients. Diabetic patients.

Design outcomes

Primary

MeasureTime frame
We expect preoperative administration of oral pregabalin or clonidine will reduce the incidence of immediate postoperative pain in patients undergoing surgery in comparison to the placebo groupTimepoint: For VAS score- baseline(immediate postoperative),1hour,2 hour,4 hour,6 hour,8 hour,12 hour,16 hour,20 hour,24 hour. For time to first rescue analgesic-immediate post operative period till complain of significant pain. For total dose of rescue analgesic- immediate post operative period till 24 hour.

Secondary

MeasureTime frame
Hemodynamic parameters like mean arterial pressure heart rate.Evaluate sensory and motor block parameters after subarachnoid block. Determine sedation. Record side effects and sedation score in all groups. Timepoint: Intraoperative hemodynamic parameters- baseline,then every 5 minute till operation lasts. Motor and sensory block characteristics- immediately after sub arachnoid blocke, at 5 minute interval till the regression of sensory and motor block. Side effects and sedation scores - baseline,at interval of 1 hour till end of 24 hour.

Countries

India

Contacts

Public ContactDr Prosenjit Mukherjee

IPGMER

ritapal1956@gmail.com9830418539

Outcome results

None listed

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