Overview
Effect of Intracervical on the Pain Associated With the Insertion of the LNG-IUS
Status:
Completed
Completed
Trial end date:
2013-07-01
2013-07-01
Target enrollment:
0
0
Participant gender:
Female
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 treatmentsPhase:
N/AAccepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
University of Sao PauloCollaborator:
Conselho Nacional de Desenvolvimento Científico e TecnológicoTreatments:
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