COMPARISON OF EFFECTS OF GABAPENTIN AND CLONIDINE ON POST-OPERATIVE PAIN AND ANXIETY IN LUMBAR SPINAL SURGERY.

NCT ID: NCT07297888

Last Updated: 2025-12-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-07-20

Study Completion Date

2024-03-20

Brief Summary

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the investigators have tested whether gabapentin is superior to clonidine top decrease the post operative pain during spinal surgeries as a part of their thesis study. the investigators are registering this study post date as the student forgot by mistake to do so.

Detailed Description

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Conditions

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Pain

Keywords

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gabapentin clonidine pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Caregivers

Study Groups

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clonide

In this group the investigators have given clonidine to the participants

Group Type ACTIVE_COMPARATOR

Gabapentin

Intervention Type DRUG

comparison of both these drugs to decrease pain

placebo

in this group no active drug was given to the participants

Group Type PLACEBO_COMPARATOR

Gabapentin

Intervention Type DRUG

comparison of both these drugs to decrease pain

gabapentin

In this group the investigators have given gabapentin to the participants

Group Type ACTIVE_COMPARATOR

Gabapentin

Intervention Type DRUG

comparison of both these drugs to decrease pain

Interventions

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Gabapentin

comparison of both these drugs to decrease pain

Intervention Type DRUG

Other Intervention Names

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clonidine

Eligibility Criteria

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Inclusion Criteria

\- Eligible participants were aged 18-60 years, classified as ASA physical status I or II, and scheduled for one or two-level lumbar laminectomy.

Exclusion Criteria

* Patients with psychiatric disorders, autoimmune diseases, local infection, BMI \>35, emergency procedures, tumour surgeries and the patients requiring the postoperative ventilation were excluded
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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All India Institute of Medical Sciences, Rishikesh

OTHER_GOV

Sponsor Role lead

Responsible Party

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ADABALA VIJAY BABU

ABabu

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Adabala Vijay Babu

Dehradun, Uttarakhand, India

Site Status

Countries

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India

Other Identifiers

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14

Identifier Type: -

Identifier Source: org_study_id