Subfertility
Conditions
Interventions
None listed
Sponsors
None
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
| Measure | Time 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
| Measure | Time 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
Outcome results
None listed