NCT02033304

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
229

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2014

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 9, 2014

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 10, 2014

Completed
22 days until next milestone

Study Start

First participant enrolled

February 1, 2014

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2014

Completed
Last Updated

May 7, 2015

Status Verified

January 1, 2013

Enrollment Period

5 months

First QC Date

January 9, 2014

Last Update Submit

May 6, 2015

Conditions

Postoperative Pain

Keywords

Cesarean sectionPainWound hyperalgesia

Outcome Measures

Primary Outcomes (1)

  • Postoperative pain

    Postoperative day1

Eligibility Criteria

Age18 Years - 60 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Women after cesarean section

You may qualify if:

  • Women undergoing spinal anesthesia

You may not qualify if:

  • women unable to cooperate
  • Women undergoing general anesthesia

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Beilinson hospital

Petach Tikvah, Israel

Location

Rabin medical center

Petach Tikvah, Israel

Location

MeSH Terms

Conditions

Pain, PostoperativePain

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsNeurologic ManifestationsSigns and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 9, 2014

First Posted

January 10, 2014

Study Start

February 1, 2014

Primary Completion

July 1, 2014

Study Completion

July 1, 2014

Last Updated

May 7, 2015

Record last verified: 2013-01

Locations

IL(2)