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The analysis of the in-vivo intratubal pressure build-up during hysterosalpingography, a feasibility study.

The analysis of the in-vivo intratubal pressure build-up during hysterosalpingography, a feasibility study.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON23488
Enrollment
10
Registered
2020-09-28
Start date
2020-10-04
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

Subfertility

Interventions

None listed

Sponsors

None
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All women scheduled for an HSG

Exclusion criteria

Exclusion criteria: Not able to provide written informed consent

Design outcomes

Primary

MeasureTime frame
The primary outcome of this study was to determine the feasibility of recording the pressure build-up within the reproductive tract during an HSG procedure, with the use of a disposable fluid syringe with an integral pressure transducer.

Secondary

MeasureTime frame
Secondary outcome measures were three pain scores on the Visual Analogue Scale for Pain (scores range from 0.0 to 10.0 cm, no pain to unbearable pain) and the fluoroscopy images of the HSG procedure.

Contacts

Public ContactInez Roest

Maxima Medisch Centrum

inez.roest@mmc.nl0630122985

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)