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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01020240
Other study ID # Unimarco
Secondary ID
Status Completed
Phase N/A
First received November 24, 2009
Last updated November 25, 2009
Start date March 2009
Est. completion date June 2009

Study information

Verified date November 2009
Source Sao Marcos University
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to promote a prevention of the complications using an elaborate guide effective and easy to understand.


Description:

The puerperium consists the period of pregnancy and postpartum cycle that the alterations provoked for pregnancy and delivery on the women organism return to your state before pregnancy. The physiotherapist can follow the puerperium since hospital phase until women has been recovered of pregnancy physiologist alterations.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date June 2009
Est. primary completion date May 2009
Accepts healthy volunteers No
Gender Female
Age group 15 Years to 35 Years
Eligibility Inclusion Criteria:

- have between 15 and 35 yeas old

- has realize an emergency or elective cesarean

- being in immediate puerperium and did not have receive any orientation

Exclusion Criteria:

- complications in delivery and postpartum

- complications with the baby

- physicologics disease

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
Avolition
- avolition for cesarean discomforts
Orientation
avolition of cesarean discomfort physiotherapy orientation
Guide
avolition of cesarean discomfort physiotherapy orientation guide orientation

Locations

Country Name City State
Brazil Sepaco Hospital São Paulo

Sponsors (1)

Lead Sponsor Collaborator
Sao Marcos University

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Analogic Visual Scale 6 months Yes
Secondary Analogic Visual Scale 6 months Yes
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