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Does pregabalin decrease pain and anesthetic medication requirement in treatment of subarchanoid haemorrhage?

Pregabalin in aneurysmal subarachnoid haemorrhage

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/10/007363
Enrollment
40
Registered
2016-10-14
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- Aneurysmal subarachnoid haemorrhage

Interventions

Intervention1: Tab Pregabalin: Tab Pregabalin 75 mg bid from admission to 24 hours after surgery Control Intervention1: Pregabalin Placebo: blank pregabalin capsules with active ingredient removed.

Sponsors

Sree Chitra Tirunal Institute of Medical Sciences and Technology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Sub arachnoid haemorrhage as evidenced by CT, CT Angiography, DSA, MR Angiogram Symptomatic headache Able to swallow oral medication Able to verbalize pain score Time period between the time of aneurysm bleed to enrolment into the study should be less than three days

Exclusion criteria

Exclusion criteria: Being on pregabalin or gabapentin derivatives in the past two weeks Pregnancy / Lactation Renal failure (Se Creat >1.4mg%) Patients with chronic pain syndromes on chronic pain medication SAH grading - WFNS grade 3, 4 & 5 ASA (American Society of Anaesthesiology) 3,4 and 5 Known allergy to Tab Paracetamol or Tab Pregabalin

Design outcomes

Primary

MeasureTime frame
fentanyl in mcg/kg (above the baseline infusion)Timepoint: at the end of surgery

Secondary

MeasureTime frame
Visual analogue scoreTimepoint: pre-induction for surgery;Visual analogue score for painTimepoint: 6, 12 and 24 hours post operation

Countries

India

Contacts

Public ContactDr Karen Ruby Lionel

Sree Chitra Tirunal Institute of Medical Sciences and Technology

karen@cmcvellore.ac.in07560961638

Outcome results

None listed

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