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OpenTrials
Completed

NCT Number: NCT04720885

Management of Large Retained Products of Conception (> 4 cm): Need for an Standardized Procedure.

Collection of relevant data form patients who were treated in the Ghent University Hospital in the context of a placental remnant lager than 4 cm, performing statistical analyzes on the collected data, reviewing the literature on the subject and formulation of a recommendation for treatment of these large placental remnants.

Completed

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Key information

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • retained products of conception larger than 4 cm in largest dimension

Exclusion criteria

  • retained products of conception 4 cm or smaller in largest dimension

Treatment and study plan

kind of surgery

Procedure

hysteroscopy, curettage, other

Primary outcomes

  1. Hysteroscopy

    Time frame: time of surgery

    Kind of surgery to remove retained products of conception

  2. Vacuum Curettage

    Time frame: time of curettage

    Kind of surgery to remove retained products of conception

  3. Polyp forceps

    Time frame: time of surgery

    Surgical instrument to remove retained products of conception

  4. Prostaglandines

    Time frame: time of surgery

    Pharmacological agent to remove retained products of conception

Sponsors and collaborators

Lead sponsor

University Hospital, Ghent

Other

Registry information

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Jan 22, 2021
Registry last updated
May 11, 2023

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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