CompletedNot Applicable

Clinical Utility of Postoperative Hemoglobin Testing

United States664 participantsStarted 2019-11-22

Plain-language summary

The purpose of this study is to evaluate how many patients have hemoglobin less than 10 g/dL at post-operative day 1

Who can participate

Age range

18 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Total vaginal hysterectomy with or without bilateral salpingectomy/oophorectomy (CPT 58260, 58262, 58263, 58270, 58290, 58291, 58292, 58294) * At least one of the following vaginal native tissue prolapse repairs * Apical repair with uterosacral ligament suspension (CPT 57283) * Apical repair with sacrospinous ligament fixation (CPT 57282) * Anterior repair (CPT 57240, 57260, 57284, 57285, 57250) * Posterior repair (CPT 45560, 56800, 56810, 57200, 57210, 57250) * Surgery by one of four fellowship trained urogynecologists at TriHealth Exclusion Criteria: * Concomitant surgical procedure by a second surgeon * Malignancy identified at the time of surgery or active malignancy * Cases converted to open hysterectomy or prolapse repairs * Prolapse repair completed robotically * Prolapse repair completed with mesh * Known coagulopathy * Patient on long term preoperative anticoagulant medication (Arixtra, Coumadin, Eliquis, Heparin, Lovenox, Pradaxa, Savaysa, Xarelto)

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Number of Subjects With POD1 Hemoglobin Less Than 10 g/dL

Timeframe: Postop Day 1

Trial details

NCT IDNCT04170764

SponsorTriHealth Inc.

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2020-05-19

Results submitted2022-10-19

View on ClinicalTrials.gov More Anaemia Postoperative trials