Office hysteroscopy compared to saline infusion sonohysterography: a randomized patient compliance study.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON19984

Enrollment

100

Registered

2005-12-29

Start date

2006-01-01

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

Indication: examination of cavum uteri

Interventions

1. Saline infusion sonography

2. Office diagnostic hysteroscopy according vaginoscopic technique.

Eligibility

Inclusion criteria

Inclusion criteria: All patients with an indication for examination of cavum uteri.

Exclusion criteria

Exclusion criteria: 1. Former office diagnostic hysteroscopy or saline infusion sonography in the past; 2. Contraindication of diagnostic hysteroscopy or saline infusion sonography.

Design outcomes

Primary

Measure	Time frame
1. Parameters for patients compliance; 2. Inconclusiveness of technique.	—

Secondary

Measure	Time frame
1. Failure rate; 2. Complication rate.	—

Contacts

Public ContactF.W. Jansen

Leiden University Medical Center (LUMC), Department of Gynaecology, P.O. Box 9600

F.W.Jansen@lumc.nl+31 (0)71 5262871

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)