Randomised controlled trial of bed rest versus no bed rest, after intra-uterine insemination, impact on pregnancy rates.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON28782

Enrollment

370

Registered

2005-09-14

Start date

2005-09-01

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alle patiënten die in de deelnemende ziekenhuizen een behandeling zullen ondergaan met intra uteriene inseminatie als therapie voor hun subfertiliteit komen in aanmerking voor de studie. Koppels komen in aanmerking voor behandeling met IUI indien de vrouw ovulatoir is met of zonder ovulatie inductie en minimaal één normaal doorgankelijke tuba heeft.

Interventions

Intra uterine insemination will be performed in spontaneous cycles as well in cycles with controlled ovarian hyperstimulation (IUI-COH). IUI will be performed in lithotomy position with Trendelenburg

Eligibility

Inclusion criteria

Inclusion criteria: All patients, receiving IUI with fresh or cryo-preserved donor- or husband’s sperm IUI with or without controlled ovarian hyper stimulation (IUI-COH), as a treatment for their subfertility will be eligible for the trial.

Exclusion criteria

Exclusion criteria: 1. Tubal pathology of both fallopian tubes; 2. Patients younger than 18 years or older than 43 years of age.

Design outcomes

Primary

Measure	Time frame
Ongoing pregnancy.	—

Secondary

Measure	Time frame
Biochemical, clinical, ectopic pregnancy.	—

Contacts

Public ContactI. Custers

Academic Medical Center (AMC), Department of Obstetrics and Gynecology, Center for Reproductive Medicine P.O. Box 22660

i.m.custers@amc.uva.nl+31 (0)20 5664355 or +31 (0)20 5669111

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)