Overview

Effect of Intracervical on the Pain Associated With the Insertion of the LNG-IUS

Status:
Completed
Trial end date:
2013-07-01
Target enrollment:
0
Participant gender:
Female
Summary
This study has the objective to evaluate the effect of Injectable intracervical anesthesia in comparison with a non-steroidal anti-inflammatory drug (NSAID) on the pain scores immediately after insertion of the levonorgestrel-releasing intrauterine system (LNG-IUS) in women without previous vaginal delivery. H0: There is no difference in terms of pain score between the treatments H1: There will be difference in terms of pain score between treatments
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
University of Sao Paulo
Collaborator:
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Treatments:
Anesthetics
Ibuprofen
Levonorgestrel
Lidocaine
Criteria
Inclusion Criteria:

- patients who wanted to use the LNG-IUS as a contraceptive

- age between 18 and 45 years

- nulliparity

- absence of previous vaginal delivery

Exclusion Criteria:

- women in categories 3 and/or 4 for LNG-IUS use according to the medical eligibility
criteria of the World Health Organization

- illicit drug and/or alcohol users

- women with allergies or contraindications to NSAIDs or lidocaine

- chronic pelvic pain of any etiology

- abnormalities in the cervix (such as fibrosis or isthmus-cervical incompetence)

- previous abortion with or without uterine curettage

- psychiatric disorders

- continued use of medications that could interfere with the pain threshold