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Pregabalin tablet for Postoperative pain in breast suregry patients

Comparison of two doses of pregabalin as Pre-emptive analgesic in reducing postoperative pain in patients undergoing breast surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/12/048101
Enrollment
86
Registered
2022-12-14
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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: Capsule Pegabalin 75 mg: Capsule Pregabalin 75mg will be given to Group A two hours prior to surgery. Intervention2: Capsule Pregabalin 150mg: Capsule Pregabalin 150 mg will be given to

Sponsors

Dr. Pooja K Subbiah
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) ASA (American Society of Anaesthesiologist) physical status 1 and 2 (ASA 1- healthy patients, ASA 2- Patients with mild to moderate systemic disease which is well under control) 2)Patients for MRM (Modified Radical Mastectomy) +/- Axillary clearance 3)Patients for breast conservative surgery.

Exclusion criteria

Exclusion criteria: 1) Allergy to Pregabalin 2)Patients not willing to participate in the study. 3)Patients having history of vertigo, dizziness. 4)ASA physical status 3 and above(ASA 3- Patients with severe systemic disease, ASA 4-Patients with severe systemic disease that is a constant threat to life, ASA 5- moribund patient who is not expected to survive, ASA 6-declared brain dead patient.) 5)Patients coming for Redo surgery. 6)Patients who have received radiation 7)Patients allergic to Inj. Diclofenac 8) Patients already on Tab.Pregabalin.

Design outcomes

Primary

MeasureTime frame
To measure postoperative pain by VAS score and analgesic requirement among breast cancer patients receiving either Capsule Pregabalin 75mg or Capsule Pregabalin 150 mg.Timepoint: Postoperative pain by VAS score (visual analogue score) at 0,1, 2,4,8,12,24hrs.

Secondary

MeasureTime frame
Postoperative sedation, nausea vomitting(PONV), dizziness.Timepoint: At Postoperative 1,2,4,8,12,24hrs

Countries

India

Contacts

Public ContactDr Pooja K Subbiah

P.D.Hinduja Hospital

poojasubbiah@gmail.com9004019533

Outcome results

None listed

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