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Clinical Trials/ISRCTN17486946
ISRCTN17486946
Completed
未知

Menstrual solutions in adolescent schoolgirls in western Kenya: a cluster randomised controlled acceptability, feasibility and safety study

Kenya Medical Research Institute0 sites750 target enrollmentDecember 16, 2014

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Kenya Medical Research Institute
Enrollment
750
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

2016 Results article in https://www.ncbi.nlm.nih.gov/pubmed/26819339 results on Prevalence of reproductive tract infections and the predictive value of girls' symptom-based reporting 2016 Results article in https://www.ncbi.nlm.nih.gov/pubmed/27881530 results on Menstrual cups and sanitary pads to reduce school attrition, and sexually transmitted and reproductive tract infections 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/36185073/ (added 04/10/2022)

Registry
who.int
Start Date
December 16, 2014
End Date
April 1, 2014
Last Updated
3 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Primary school girls, in classes 5 upwards
  • 2\. Attend a study school
  • 3\. Reached menarche, experienced a minimum of three menses
  • 4\. Are aged 14\-16 years at enrolment
  • 5\. Resident in the health and demographic surveillance system study area
  • 6\. Parents/guardian provided written informed consent
  • 7\. Participating girl provided written informed assent

Exclusion Criteria

  • 1\. Not attending primary school, or below class 5
  • 2\. Not reached menarche or experienced minimum of 3 menses
  • 3\. Are outside the study age (14\-16 years at enrolment)
  • 4\. Not resident in health and demographic surveillance system study area
  • 5\. Do not attends one of the study schools
  • 6\. Parent/guardian refused informed consent
  • 7\. Participant refused informed assent
  • 8\. Participant declares presence of an intrauterine device;
  • 9\. Participants has a severe physical / learning disability preventing informed consent or ability to participate
  • 10\. Participant has suffered from toxic shock syndrome;

Outcomes

Primary Outcomes

Not specified

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