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OpenTrials
Completed

NCT Number: NCT01165814

Naproxen Versus Tramadol for Post Cesarean Pain Control

Oral naproxen might be more efficacious for post-cesarean pain-control and have better side-effects profile than oral tramadol.

Completed

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Key information

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Bnai Zion Medical Center

Haifa, Israel

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • all patients after cesarean section

Exclusion criteria

  • emergent CS
  • hypersensitivity to drug
  • drug abuse

Treatment and study plan

Naproxen Tramadol

Drug

Primary outcomes

  1. Pain Score

Secondary outcomes

  1. Side effects

Sponsors and collaborators

Lead sponsor

Bnai Zion Medical Center

Other Gov

Registry information

Official study title

Oral Naproxen Versus Oral Tramadol for Analgesia After Cesarean Delivery - A Randomized Controlled Trial

Important dates

Study start
2006
Primary completion
2009
Study completion
2009
First posted
Jul 20, 2010
Registry last updated
Jul 20, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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