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Intracervical Anesthesia and Pain Associated With Intrauterine Contraceptive Insertion

NCT03111342 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2019-08-01

No results posted yet for this study

Summary

The primary aim of our study is to evaluate the effect of intracervical anesthesia on pain scores immediately following levonorgestrel-releasing intrauterine system (LNG-IUS) insertion in nulligravida women.

Conditions

  • Pain, Acute
  • Anesthesia, Local
  • IUD Insertion Complication

Interventions

DRUG

Anesthesia

A 2% lidocaine without vasoconstrictor injection into the cervix

PROCEDURE

Dry-needling

A placement of thin needle into the cervix without substance injection

Sponsors & Collaborators

  • University of Campinas, Brazil

    collaborator OTHER

  • University of Sao Paulo

    lead OTHER

Principal Investigators

  • Carolina S Vieira, MD, PhD · University of Sao Paulo

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2017-06-01
Primary Completion
2018-08-30
Completion
2018-08-31

Countries

  • Brazil

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 NCT03111342 on ClinicalTrials.gov