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OpenTrials
Completed

NCT Number: NCT04791020

Topic Cervical Anesthesia Plus Paracervical Blockade for Pain Control During Endouterine Manual Aspiration

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

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Key information

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Saint Thomas H

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 lidocain

Treatment and study plan

Lidocain topical + paracervical blockade

Drug

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

Lidocaine topical

Drug

5mL of lidocaine gel applied topically to cervix previous to clamping, No paracervical blockade will be applied.

Primary outcomes

  1. Global evaluation of pain

    Time frame: 5 minutes post procedure

    Visible 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 Cervical Anesthesia Plus Paracervical Blockade vs. Topical Cervical Anesthesia Alone for Pain Control During Endouterine Manual Aspiration

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Mar 10, 2021
Registry last updated
Oct 6, 2021

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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