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analgesic effects of a drug in thoracic surgeries

A randomized clinical trial on the effects of oral Pregabalin compared with placebo in acute postoperative pain in patients who undergo Thoracotomy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014110210900N4
Enrollment
60
Registered
2016-04-05
Start date
2014-01-19
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

Acute pain. Acute pain

Interventions

Intervention 1: In intervention group, 300 mg pregabalin is administered orally as an analgesic, 2 hours before surgery. Intervention 2: In control group placebo (a capsule similar to the drug without
Treatment - Drugs
In intervention group, 300 mg pregabalin is administered orally as an analgesic, 2 hours before surgery
In control group placebo (a capsule similar to the drug without any effective substance) is administered.

Sponsors

Vice chancellor for research, Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Patients, who are admitted for thoracic surgery, age 20 to 65 year. Exclusion criteria: pregnancy, history of allergy to pregabalin, history of treatment with pregabalin or gabapentin, history of chronic pain syndromes and painkiller consumption, addiction to alcohol or drugs, allergy to pethidine, psychiatric drug consumption, surgery lasting more than 4 hours, uncontrolled blood pressure, history of convulsion and the patients who had preoperative pain based on the visual analogue scale (VAS) had preoperative pain.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: At the end of operation and transferring to recovery room, the score of pain is measured every 15 minutes for an hour and after transporting to ward, every 4 hours for 24 hours. Method of measurement: VISUAL ANALOGUE SCALE.

Secondary

MeasureTime frame
The dose of analgesic. Timepoint: during and after surgery. Method of measurement: recording the dose and frequency of administration.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHosein Sattari

Kerman University of Medical Sciences

hosattari@gmail.com+98 34 3223 5011

Outcome results

None listed

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