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CompletedNCT03381612FCUpdated Dec 22, 2017

Prevalence of Female Circumcision Among Young Women in Beni-Suef, Egypt

An observational study in Woman Abuse, sponsored by Beni-Suef University. Completed at 1 site in Egypt. Open to female participants aged 12 Years to 25 Years. Per ClinicalTrials.gov, last updated 2017-12-22.

Sponsored by Beni-Suef University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
3,353
Ages
12 Years to 25 Years
Sex
Female
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Study summary

Female circumcision (FC) is a deeply-rooted practice in Egypt with deblitating physical and psychological consequences, however the previous two decades witnessed sincere efforts to counterfight this practice. The objective of this study is to investigate the prevalence of circumcision among young women (12-25 years) in Beni-Suef , Egypt.

Read the detailed description

This cross-sectional study was conducted on a total of 3353young women residing urban and rural quraters in Beni-Suef City. Data was collected usinga questionnaire that included information about the socio-demographic charcteristics of the women, their gynecological data, exposure to FC, and complaints associated with menses during the previous year.

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Conditions studied

  • Woman Abuse

Keywords

  • Female circumcision, Young Women, Dysmenorrhea,Dysuria
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In context

Dysmenorrhea

430 studies on the registry are indexed under Dysmenorrhea; 107 are open to participants now.

This study's enrollment of 3,353 is above the median of 107 across 58 observational studies indexed under Dysmenorrhea.

Browse Dysmenorrhea studies →

Lead sponsor

Beni-Suef University is the lead sponsor of 349 studies on the registry; 125 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
12 Years to 25 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

The urban Metropolitan of Beni-Suef City was classified according to the socioeconomic level of its quarters to low, middle, and high levels. Out of each level, one quarter was selected randomly, by a card withdrawal, where households residing these quarters were chosen using a random start. For the rural villages surrounding the urban Metropolitan, three villages were selected randomly; one on the road to the North, one on the road to the West, and the last one on the road to the South. Each village was clustered roughly into two sites; one to the East of the water channel and one to the West of the same water channel.

In both urban and rural areas, a trained team of data collectors visited the selected households. Householders were informed briefly of the study and the residing women aged between 12 and 25 years were invited to participate and then interviewed.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Young women aged 12 to 25 years living in Beni-Suef city of Egypt. the urban Metropolitan of Beni-Suef City was classified according to the socioeconomic level of its quarters to low, middle, and high levels. Out of each level, one quarter was selected randomly, by a card withdrawal, where households residing these quarters were chosen using a random start. For the rural villages surrounding the urban Metropolitan, three villages were selected randomly; one on the road to the North, one on the road to the West, and the last one on the road tothe South. Each village was clustered roughly into two sites; one to the East of the water channel and one to the West of the same water channel

Exclusion criteria

Exclusion Criteria:

  • Women from other places in Egypt.
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Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
3,353 participants (actual)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Gynecological manifestations measured by a questionnaire.

    A questionnaire included questions about the manifestations associated with menses and average duration of dysmenorrhea during the previous year.

    Time frame: one year

Secondary outcomes

  1. social status measured by a questionnaire

    A questionnaire included questions about age at menarche, social, educational and work status.

    Time frame: one year

Other outcomes

  1. working status measured by a questionnaire

    For data collection, a questionnaireof two sections was prepared;the first section included socio-demographic data, social status, working status and educational level,age at menarche, menstrual cycle duration and flow days, in addition to exposure to circumcision. The second section includedquestions about the manifestations associated with menses and average duration of dysmenorrhea

    Time frame: One year

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Study locations

1 site
  • Beni-Suef University
    Cairo, 018, Egypt
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References and documents

Publications

  • Burstyn L. Female circumcision comes to America. The Atlantic Monthly. 1995; pp 28-35.
  • Moustafa T. Conflict and cooperation between the state and religious institutions in contemporary Egypt. International Journal of Middle East Studies 2000; 32:3-22.
  • Sayed GH, Abd el-Aty MA, Fadel KA. The practice of female genital mutilation in upper Egypt. Int J Gynaecol Obstet. 1996 Dec;55(3):285-91. doi: 10.1016/s0020-7292(96)02753-1. PubMed 9003955 ↗

Individual participant data

Plan to share: No

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Apr 2017 to primary completion in Jul 2017, 3 months.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 8, 2017
First posted
Dec 22, 2017
StartActual
Apr 3, 2017
Primary completionActual
Jul 15, 2017
CompletionActual
Jul 15, 2017
Last update
Dec 22, 2017
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Dec 22, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03381612
Responsible party
Nesreen Abdel Fattah Abdullah Shehata (Assistant Professor of Obstetrics and Gynecology, Beni-Suef University) — Principal investigator
First posted
Dec 22, 2017
Start date
Apr 3, 2017
Primary completion
Jul 15, 2017
Completion
Jul 15, 2017
Last update
Dec 22, 2017

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2017. You cannot join it, but the record below documents what was studied.

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