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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02863614
Other study ID # CAAE: 36622214.5.0000.5440
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2015
Est. completion date May 2017

Study information

Verified date May 2018
Source University of Sao Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate whether Ibuprofen alone or combined with lorazepam reduce the pain associated with endometrial scratching/injury.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date May 2017
Est. primary completion date May 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Women aged = 18 years undergoing assisted reproduction (IUI, IVF/ICSI, frozen embryo transfer)

- Being submitted to endometrial scratching/injury with a Pipelle on the first four days of the menstrual cycle.

- Not have performed endometrial scratching in the last 90 days.

Exclusion Criteria:

- None

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ibuprofen 600 mg

Lorazepam 1 mg

Placebo


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Sao Paulo

Outcome

Type Measure Description Time frame Safety issue
Primary Maximum pain during procedure Evaluated by both visual analog scale (10 cm) and numeric verbal scale (0 to 10). 5 minutes
Secondary Pain after the procedure Evaluated by both visual analog scale (10 cm) and numeric verbal scale (0 to 10). 5 minutes
Secondary Rejection to a new procedure Evaluated by a 5-point Likert scale, commenting on this sentence: "I would repeat this procedure if it were indicated". 1 = I fully agree; 2 = I agree; 3 =Neither agree nor disagree; 4 = Disagree; 5 = Strongly Disagree. 5 minutes
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