Skip to main content
OpenTrials
Completed

NCT Number: NCT03279666

Biopsy Size and Pain Perception During Colposcopic Biopsy

The investigators will investigate patients pain and biopsy size during colposcopic biopsy. The investigators will use tenaculum randomized patient with or without intracervical blockage.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Pain Uterus Tenaculum

Age range

18 year–80 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Cihan Comba

Istanbul, 34000, Turkey (Türkiye)

About this study

The study was designed four arms. The investigators will perform colposcopy because of various causes. The first arm is used tenaculum and performed intracervical blockage. The second arm is not used tenaculum and performed intracervical blockage. The third arm is used tenaculum and not performed intracervical blockage. The fourth arm is not used tenaculum and not performed intracervical blockage and then we will study patients pain and biopsy size during colposcopic biopsy. Pain reduce and biopsy size are very important for patient and diagnose of the cervix cancer.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 18-80 year-old women who had colposcopic biopsy

Exclusion criteria

  • Had orthopedical problems
  • Analgesic allergy
  • Have previous cone biopsy
  • Analgesic use until six hours before colposcopy
  • Advanced cervicovaginal atrophy
  • Linear Visual Analog Score for pain is used

Treatment and study plan

Tenaculum replacement

Other

Tenaculum replacement during colposcopic biopsy

Primary outcomes

  1. Patients' Biopsy Sizes

    Time frame: 6 months

    Are patients' biopsy sizes associate with tenaculum. Milimeter will be used for biopsy size.

  2. Patients' Biopsy Sizes

    Time frame: 6 months

    Are patients' biopsy sizes associate with analgesic. Milimeter will be used for biopsy size.

Secondary outcomes

  1. Patients' pain perceptions

    Time frame: 6 months analgesic

    Are patients' pain perceptions associate with analgesic. Linear Visual Analog Scale will be used for pain perception.

  2. Patients' pain perceptions

    Time frame: 6 months

    Are patients' pain perceptions associate with teanaculum. Linear Visual Analog Scale will be used for pain perception.

Sponsors and collaborators

Lead sponsor

Bakirkoy Dr. Sadi Konuk Research and Training Hospital

Other Gov

Registry information

Official study title

A Randomized Controlled Study: Patients' With or Without Tenaculum Placement and Intracervical Blockage/or Not During Colposcopic Biopsy

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Sep 12, 2017
Registry last updated
Jun 8, 2018

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.

Related clinical trials

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