Pain in Diagnostic Hysteroscopy

The objective of this study is to assess which factors influence the pain perceived during diagnostic anesthesia-free hysteroscopy.

Completed

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Key information

Conditions

Pain in Diagnostic Hysteroscopy Neurologic Manifestations Pain Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year–80 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Arbor Vitae Endoscopic Centre

Rome, Italy, 00191

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

female gender
diagnostic hysteroscopy indication
italian-speaking patients

Exclusion criteria

patients who had previously undergone a diagnostic hysteroscopy
patients who had been previously undergone to cervical surgery
ongoing pregnancy
cervical carcinoma
pelvic inflammatory disease
excessive uterine bleeding
performance of an endometrial biopsy during the procedure

Treatment and study plan

diagnostic hysteroscopy

Procedure

Primary outcomes

Evaluation of pain during diagnostic hysteroscopy by Visual Analogue Scale.

Time frame: 5 minutes after the procedure.

Sponsors and collaborators

Lead sponsor

Sandro Gerli

Other

Registry information

Official study title

Pain in Diagnostic Hysteroscopy: a Multivariate Analysis.

Important dates

Study start: 2013
Primary completion: 2014
Study completion: 2014
First posted: Jun 10, 2013
Registry last updated: Feb 6, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed