Skip to main content
Clinical Trials/IRCT2017041810426N16
IRCT2017041810426N16
Completed
未知

Evaluation of the effect of consultation based on Bristol tool on self-efficacy and continuation of breast- feeding among primi-parous women undergoing cesarean section.

Hamadan University of Medical Sciences0 sites80 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Breast- feeding disorders among mothers undergoing Cesarean section.
Sponsor
Hamadan University of Medical Sciences
Enrollment
80
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Cesarean section delivery; primiparous; literacy; Residency in Hamadan city; Having a mobile number for follow\-ups; Singleton birth and term delivery. Exclusion criteria: Inability to do breastfeeding according to physician’s approval; Problems after cesarean section such as bleeding and anesthesia related problems; Underlying disease in mother such as cardiac, pulmonary, chronic and infection diseases; Addiction; Neonatal abnormality and diseases.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Similar Trials