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Ultrasound Guided Intra-uterine Device Insertion

Not Applicable
Completed
Conditions
Contraception
Registration Number
NCT02393495
Lead Sponsor
Woman's Health University Hospital, Egypt
Brief Summary

Different studies have been made in an attempt to reduce the pain and the duration of the process of outpatient insertion of the intrauterine device. in this trial, the investigators aim to insert the IUD under ultrasonographic guidance, which can help to reduce the pain, decrease the process of insertion, in addition, it reduces the incidence of malposition of IUD as well as the risk of complications.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
102
Inclusion Criteria
  • Females desiring contraception with the use of IUD
Exclusion Criteria
  • Are pregnant or think they may be pregnant
  • Septic pregnancy or abortion
  • Have unexplained abnormal vaginal bleeding
  • Have untreated cervical cancer
  • Have malignant gestational trophoblastic disease
  • Have uterine cancer
  • Have uterine abnormalities
  • Have or may have had a pelvic infection within the past three months
  • Have or may have any sexually transmitted disease
  • Have pelvic tuberculosis
  • Are postpartum between 48 hours and 4 weeks
  • Have benign gestational trophoblastic disease
  • Have ovarian cancer
  • Have AIDS (unless clinically well on anti-retroviral therapy)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Assessment of degree of pain during IUD insertion6 months

Pain will be assessed by the use of visual analog scale, Pain rating scale

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Kasr el ainy hospital

🇪🇬

Cairo, Egypt

Kasr el ainy hospital
🇪🇬Cairo, Egypt

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