Last reviewed · How we verify

NCT01541241: IUD

Study About Patients Using Copper Intrauterine Device

Completed Last updated 4 December 2020
What this trial tests

trial in Copper Intrauterine Device Induced Bleeding in 100 participants. Completed in 30 May 2012.

Timeline
2 January 2012
Primary endpoint
28 February 2012
30 May 2012

Quick facts

Lead sponsorEgymedicalpedia
StatusCompleted
Study typeOBSERVATIONAL
Enrollment100
Start date2 January 2012
Primary completion28 February 2012
Estimated completion30 May 2012
Sites1 location across Egypt

Conditions studied

Sponsor

Egymedicalpedia — full company profile →

Who can join

Adults 18 to 35, female only, with Copper Intrauterine Device Induced Bleeding. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

THE AIM OF THE this study is to assess the hemodynamic changes of uterine artery in patients with CIUD induced bleeding by using transvaginal color Doppler indices (uterine artery resistance index and pulsatility index) to prove the relationship between these changes and bleeding in these patient .

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other Egymedicalpedia trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01541241.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing