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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03397082
Other study ID # Mhst2014-13
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2014
Est. completion date December 1, 2014

Study information

Verified date December 2018
Source Saint Thomas Hospital, Panama
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To compare the effectiveness of lidocaine gel plus paracervical blockade vs. Paracervical blockade alone in the management of pain during endouterine manual aspiration.


Recruitment information / eligibility

Status Completed
Enrollment 86
Est. completion date December 1, 2014
Est. primary completion date September 30, 2014
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Need for a endouterine manual aspiration (incomplete abortion or gynecological bleeding).

Exclusion Criteria:

- Allergy to lidocaine.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Lidocaine gel
5mL of lidocaine gel applied topically to cervix previous to clamping and paracervical blockade.
Placebo
5mL of sterile gel applied topically to cervix previous to clamping and paracervical blockade.

Locations

Country Name City State
Panama Saint Thomas Maternity Hospital Panama

Sponsors (1)

Lead Sponsor Collaborator
Saint Thomas Hospital, Panama

Country where clinical trial is conducted

Panama, 

Outcome

Type Measure Description Time frame Safety issue
Primary Global evaluation of pain Visual scale of pain evaluation 5 minutes post procedure
Secondary Adverse reaction Presence of adverse effects to the drug used (lidocaine gel) 5 minutes post procedure
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