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NCT06149598Completed

Coughing at Time of Cervical Biopsy

Pain Reduction by Forced Coughing During Colposcopy Guided Cervical Biopsies: a Randomized Controlled Pilot Study

Source: ClinicalTrials.gov · Last updated 4 Mar 2025

Brief summary (registry, in English)

To investigate the effect of coughing as an intervention to reduce pain in colposcopy guided biopsy.

Status (registry)
Completed
Study type
Interventional
Enrollment
30 (actual)
First submitted
19 Nov 2023
Start date
2 Jan 2024
Primary completion date
30 Apr 2024
Lead sponsor
Zydolab - Institute of Cytology and Immune Cytochemistry
NCT number
NCT06149598

What you commit to

  • Study type: Interventional
  • Participants enrolled: 30
  • From 2 Jan 2024 to the primary completion date, 30 Apr 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Chronic use of pain medications or psychotropic medications or other medications that may have an influence on the sensation of pain

Other illness

  • Vaginal bleeding at the time of examination
  • known anxiety disorders or depressive disorders
  • Patients with a chronic or acute illness that influences the perception of pain or lead to permanent pain due to the disease itself
  • psychosomatic illnesses

Other

  • Performing only one biopsy or more than two biopsies
  • Performing an endocervical curettage (biopsy on the endocervix)
  • inadequate colposcopy
  • Cervix uteri cannot be fully visualized
  • Pregnancy
  • Patients with insufficient German language skills
  • Treatments already carried out on the cervix uteri

Who the study is looking for

  • Completed 18 years of age
  • written informed consent
  • first colposcopy
  • Clinically indicated colposcopy in case of an abnormal PAP smear or screening result and/or clinical abnormalities on the cervix uteri
  • Necessity to take exactly two biopsies

Age in the registry: 18 years to 80 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Zydolab - Institute of Cytology and Immune Cytochemistry
Coordinator of this site? Confirm its status
DortmundGermanyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.