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OpenTrials
Completed

NCT Number: NCT06924437

Evaluation of the Uterine Cavity After Operative Hysteroscopy

This study will focus on evaluation of the uterine cavity after operative hysteroscopy using three dimensional transvaginal ultrasonography and office hysteroscopy to detect and residual or recurrent abnormalities or intrauterine adhesions to optimize the results of operative hysteroscopy in different uterine pathologies such as uterine polyps, fibroids, adhesions in addition to mullerian anomalies especially uterine septum .

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients in reproductive age group
  • Patients already selected for operative hysteroscopy
  • Patients accepted to share in the study
  • Patients accepted to come for follow up ( within 3 months after the initial operative procedure, at least after 4 weeks

Exclusion criteria

  • Patients outside the age of reproduction
  • Patients with negative findings at operative hysteroscopy
  • Patients refused to share in the study
  • Patients not available for follow up
  • Infection
  • pregnancy or design of pregnancy

Treatment and study plan

Primary outcomes

  1. Rate of bias in 3 dimensional ultrasonography compared to office hysteroscopy

    Time frame: one year

    Comparing three dimensional ultrasonography and office hysteroscopy for uterine cavity evaluation after operative hysteroscopy as regards accuracy, pain score, and cost-effectiveness of each method.

Secondary outcomes

  1. Concentration of the risks and benefits between 3 dimensional ultrasonography and office hysteroscopy

    Time frame: 1 year

    To compare three dimensional ultrasonography with office hysteroscopy in evaluation of the uterine cavity after operative hysteroscopy and if the non invasive procedure can replace the invasive one or not

Other outcomes

  1. Number of participants with infertility , abnormal uterine bleeding and dysparunia

    Time frame: 1 year

    all cases in this study already underwent operative hysteroscopy for a specific complaint

Sponsors and collaborators

Lead sponsor

Sohag University

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 11, 2025
Registry last updated
Jul 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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