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Effects of oral gabapentin versus oral placebo on controlling of pain after central venous catheter insertion

Effects of oral gabapentin versus oral placebo on controlling of pain after central venous catheter insertion: a double-blind randomized clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120215009014N535
Enrollment
60
Registered
2024-11-07
Start date
2024-11-10
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Pain. Pain, not elsewhere classified

Interventions

Intervention 1: Intervention group: Gabapentin tablets 1200 mg one hour before central venous catheter insertion and then 600 mg 3 times a day for a maximum of one week. Intervention 2: Control group:

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age 18 to 60 years Candidate for central venous catheter operation

Exclusion criteria

Exclusion criteria: Body mass index above 30 Treated with narcotic drugs Kidney or liver disorder Pregnancy

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: At 12, 24, 48 and 72 hours after central venous catheter insertion and also at the time of discharge. Method of measurement: Using Visual Analog Scale (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSalman Shakiba

Hamedan University of Medical Sciences

bazvand_salman@yahoo.com+98 81 3838 0572

Outcome results

None listed

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