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OpenTrials
Completed

NCT Number: NCT03397082

Topic Cervical Anesthesia for Pain Control During Endouterine Manual Aspiration

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

Completed

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Key information

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Saint Thomas Maternity Hospital

Panama City, Panama

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Allergy to lidocaine.

Treatment and study plan

Lidocaine gel

Drug

5mL of lidocaine gel applied topically to cervix previous to clamping and paracervical blockade.

Placebo

Drug

5mL of sterile gel applied topically to cervix previous to clamping and paracervical blockade.

Primary outcomes

  1. Global evaluation of pain

    Time frame: 5 minutes post procedure

    Visual scale of pain evaluation

Secondary outcomes

  1. Adverse reaction

    Time frame: 5 minutes post procedure

    Presence of adverse effects to the drug used (lidocaine gel)

Sponsors and collaborators

Lead sponsor

Saint Thomas Hospital, Panama

Other

Registry information

Official study title

Topic Use of Lidocaine Gel Plus Paracervical Blockade vs. Paracervical Blockade Alone for Pain Control During Endouterine Manual Aspiration: A Randomized Controlled Trial

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Jan 11, 2018
Registry last updated
Dec 11, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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