Skip to main content
OpenTrials
Completed

NCT Number: NCT02033304

Factors Predicting Postoperative Cesarean Section Pain

In spite of identical analgesic protocols, parturients suffer different levels of pain postoperative lay. In this study we hope to identify factors which influence the perception of pain including preoperative anxiety, sleep quality and local anesthesia injection pain.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–60 year

Sex eligibility

Female

Study type

Observational

Primary location

Beilinson hospital, Petach Tikvah, Israel

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Women undergoing spinal anesthesia

Exclusion criteria

  • women unable to cooperate
  • Women undergoing general anesthesia

Treatment and study plan

Primary outcomes

  1. Postoperative pain

    Time frame: Postoperative day1

Sponsors and collaborators

Lead sponsor

Rabin Medical Center

Other

Registry information

Official study title

Analysis of Factors Predicting Postoperative Pain and Wound Hyperalgesia After Cesarean Section

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Jan 10, 2014
Registry last updated
May 7, 2015

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.

Published trials that share one or more normalized conditions with this study.