Topic Cervical Anesthesia for Pain Control During Endouterine Manual Aspiration

Saint Thomas Hospital (HST)

Status: Completed

Conditions: Pain

Treatments: Drug: Lidocaine gel; Drug: Placebo

Study type: Interventional

Funder types: Other

Identifiers

NCT03397082

Mhst2014-13

Details and patient eligibility

About

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

Enrollment: 86 patients

Sex: Female

Volunteers: No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

• Allergy to lidocaine.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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86 participants in 2 patient groups, including a placebo group

Lidocaine + Paracervical blockade

Experimental group

Description:

5 minutes previous to endouterine manual aspiration, 5mL of lidocaine gel was applied plus standard paracervical blockade.

Treatment:

Drug: Lidocaine gel

Placebo + paracervical blockade

Placebo Comparator group

Description:

5 minutes previous to endouterine manual aspiration, standard paracervical blockade was applied plus placebo gel (KY).

Treatment:

Drug: Placebo