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The Effect of Gabapentin , Celecoxib and Their Combination on Pain and Systemic Symptoms after laminectomy

The Comparison Effect of Gabapentin , Celecoxib and Their Combination on Pain and Systemic Symptoms after laminectomy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015071222870N3
Enrollment
152
Registered
2015-09-18
Start date
2015-08-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

laminectomy. Vertebral column

Interventions

Intervention 1: Intervention 2: In Celecoxib group, 400 mg Celecoxib capsule 2 hrs before surgery and 6 hrs after surgery is given. Intervention 2: Intervention 3: In Gabapentin pulse Celecoxib group,
Treatment - Drugs
Intervention 2: In Celecoxib group, 400 mg Celecoxib capsule 2 hrs before surgery and 6 hrs after surgery is given.
Intervention 3: In Gabapentin pulse Celecoxib group, 300 mg Gabapentin capsule pulse 200 mg Celecoxib 2 hrs before surgery and 6 hrs after surgery is given.
Control 1: In placebo group, capsule contain starch 2 hrs before surgery and 6 hrs after surgery is given.
Intervention 1: In Gabapentin group, 600 mg Gabapentin capsule 2hrs before surgery and 6 hrs after surgery is given.

Sponsors

Ilam University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 20-60; same surgeon and anesthesia. Exclusion criteria: drug abuse; history of allergic reaction to any of the study drugs; under use of non-steroidal anti-inflammatory analgesic; pregnancy; cardiovascular; metabolic; respiratory; peptic ulcer and renal failure or coagulation abnormalities.

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Pruritus. Timepoint: After surgery. Method of measurement: Questionnaire.;The first movement time. Timepoint: During 24 h after surgery. Method of measurement: Questionnaire.

Primary

MeasureTime frame
Shivering. Timepoint: During recovery. Method of measurement: Checklist and VAS.;Pain. Timepoint: 2,4,6,8,12,16,24 hrs after surgery. Method of measurement: Visual Analogue Scale (VAS).;Drug consumption. Timepoint: During 24 hrs after surgery. Method of measurement: Mg.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Khani

Ilam University of Medical Sciences

nimakhani@gmail.com; khani-a@medilam.ac.ir+98 84 3333 7259

Outcome results

None listed

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