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efficacy of hyoscine on dilation of the cervix

Evaluation the efficacy of hyoscine on dilation of the cervix before hysteroscopy: an open-labeled randomized control trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220822055772N1
Enrollment
84
Registered
2023-04-03
Start date
2023-04-21
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Menopausal women. Unspecified menopausal and perimenopausal disorder

Interventions

Intervention 1: Intervention group: The intervention group is candidate to receive hyosine vaginal tablets. 2 hours before the hysteroscopy procedure, two hyoscine tablets (10 mg, manufactured by Pors

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patient's willing to participate in study Menopausal women who are planed for hysteroscopy and dilator number 4 does not pass from cervix Negative past cervical surgery Negative allergy history about Hyoscine Negative past medical history about cancers, obstructive bowel disease and cardiopulmonary disease

Exclusion criteria

Exclusion criteria: not willing to participate in study Sensitivity to hyoscine

Design outcomes

Primary

MeasureTime frame
Cervical dilation. Timepoint: 2 hours after medication. Method of measurement: bogie number 4.

Secondary

MeasureTime frame
Hyoscine side effect. Timepoint: after operation. Method of measurement: physician submission.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHanieh Najafiarab

Shahid Beheshti University of Medical Sciences

Haniye.najafiarab@gmail.com+98 21 7758 2543

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026