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Clinical Trials/ISRCTN56764412
ISRCTN56764412
Completed
Not Applicable

A prospective randomized study for pain assessment during outpatient hysteroscopy using room temperature versus warm normal saline as distention medium.

Central Clinical Hospital of Ministry of the Interior in Warsaw (CSK MSW) Department Obs and Gyn0 sites100 target enrollmentJuly 24, 2015
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ConditionsOutpatient hysteroscopySurgeryHysteroscopy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Outpatient hysteroscopy
Sponsor
Central Clinical Hospital of Ministry of the Interior in Warsaw (CSK MSW) Department Obs and Gyn
Enrollment
100
Status
Completed
Last Updated
9 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 24, 2015
End Date
TBD
Last Updated
9 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Central Clinical Hospital of Ministry of the Interior in Warsaw (CSK MSW) Department Obs and Gyn

Eligibility Criteria

Inclusion Criteria

  • •All patients aged over 18 years referred for hysteroscopy for diagnosis of abnormal endometrium on ultrasound, endometrial polyps and uterine bleeding were included in the study. All participants had a pelvic ultrasound examination to confirm the initial diagnosis.

Exclusion Criteria

  • •Women with a possible pregnancy, lower genital tract infections, gestational trophoblastic disease, presence of endocervical polyps visualized on a speculum examination, asthma, acute porphyria, hepatitis, renal failure, lactation and oversensitivity to one of the agents or their elements were excluded.
  • •Patients with endometrial polyps measuring more than 30mm were excluded and referred for operative hysteroscopy under anesthesia.

Outcomes

Primary Outcomes

Not specified

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