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Psychosocial and Clinical Characteristics Predicting Women's Acceptance of Office Hysteroscopy

NCT02543515 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2017-02-02

No results posted yet for this study

Summary

Study type:

Observational, prospective.

Objectives:

Primary:

Identify psychosocial and clinical factors that predispose to the occurrence of pain following office hysteroscopy

Secondary:

Stratify risk factors for pain previous Cesarean section and pain score repeat C section and pain score post-menopausal and pain score type of delivery and pain score body mass index and pain score history of dysmenorrhea and pain score, abnormal uterine bleeding and pain score previous surgery upon uterine cervix and pain score Characterize women's psychosocial profile and pain score Establish anxiety as a factor influencing pain perception using (State-Trait Anxiety Inventory for Adults).

Determine if there is a specified population who would benefit from procedure under anaesthesia

Conditions

  • Pelvic Girdle Pain

Interventions

PROCEDURE

office hysteroscopy

diagnostic procedure

Sponsors & Collaborators

  • Marta Fernandes, M.D. MSc

    collaborator UNKNOWN

  • Sonia Gonçalves, M.D

    collaborator UNKNOWN

  • José Damasceno Costa, M.D.

    collaborator UNKNOWN

  • Antonio Pipa, M.D.

    collaborator UNKNOWN

  • Raquel Oliveira, MSc.

    collaborator UNKNOWN

  • nurse Catarina Mota

    collaborator UNKNOWN

  • nurse Carla Santos

    collaborator UNKNOWN

  • Centro Hospitalar Tondela-Viseu

    lead OTHER

Principal Investigators

  • Antonio Paulo, MD · Centro Hospitalar Tondela-Viseu

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2015-09-30
Completion
2015-11-30

Countries

  • Portugal

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02543515 on ClinicalTrials.gov