Skip to content

Evaluation of the Effectiveness of pregabalin on chronic pain

Evaluation of the Effectiveness of Oral Pregabalin on Chronic Pain in Patients with Blunt Chest Trauma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251205068217N1
Enrollment
50
Registered
2025-12-20
Start date
2025-12-22
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Chronic pain in patients with blunt chest trauma. Chronic pain due to trauma

Interventions

Intervention 1: Intervention group: patients in this group will receive oral pregabalin, with an initial dose of 25 mg once daily. In addition, patients will receive naproxen 250 mg orally twice daily

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Chronic thoracic pain (persistent pain in the thoracic region for at least 12 weeks) following blunt chest trauma Age between 18 and 75 years Failure of previous conservative management, including physical therapy and non-opioid pain medications

Exclusion criteria

Exclusion criteria: History of allergic reactions to pregabalin, NSAIDs, or any of their components Presence of severe renal impairment (estimated glomerular filtration rate less than 30 ml/min). History of bleeding or peptic ulcer in the past six months Current or previous use of pregabalin or gabapentin in the past month Presence of significant psychiatric disorders, including major depression and anxiety disorders, that may interfere with participation in the study Pregnant or breastfeeding women. Patients with a history of substance abuse or current opioid use Patients with a history of epilepsy or any other neurological disorder that may contraindicate the use of pregabalin

Design outcomes

Primary

MeasureTime frame
Intensity of pain. Timepoint: Patients will attend study visits at baseline, 2 weeks, 4 weeks, 8 weeks, and 12 weeks. Method of measurement: Assessing pain intensity using a Numerical Rating Scale (NRS).

Secondary

MeasureTime frame
Incidence and severity of side effects. Timepoint: Patients will attend study visits at baseline, 2 weeks, 4 weeks, 8 weeks, and 12 weeks. Method of measurement: A checklist for recording possible drug side effects, which includes drowsiness, dizziness, abdominal pain, nausea, vomiting, allergic skin reactions, peripheral edema, and blurred vision, is completed at each visit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShiva Bahremand

Kerman University of Medical Sciences

bahremand.shiva@gmail.com+98 34 3281 8754

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026