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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03397082 |
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Date of registration:
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02/01/2018 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Topic Cervical Anesthesia for Pain Control During Endouterine Manual Aspiration
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Scientific title:
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Topic Use of Lidocaine Gel Plus Paracervical Blockade vs. Paracervical Blockade Alone for Pain Control During Endouterine Manual Aspiration: A Randomized Controlled Trial |
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Date of first enrolment:
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August 1, 2014 |
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Target sample size:
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86 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03397082 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Panama
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Contacts
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Name:
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Osvaldo Reyes, Md |
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Address:
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Telephone:
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Email:
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Affiliation:
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Saint Thomas Maternity Hospital |
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Name:
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Ariel Veces |
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Address:
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Telephone:
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Email:
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Affiliation:
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Saint Thomas Maternity Hospital |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Need for a endouterine manual aspiration (incomplete abortion or gynecological
bleeding).
Exclusion Criteria:
- Allergy to lidocaine.
Age minimum:
N/A
Age maximum:
N/A
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Pain
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Intervention(s)
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Drug: Lidocaine gel
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Drug: Placebo
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Primary Outcome(s)
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Global evaluation of pain
[Time Frame: 5 minutes post procedure]
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Secondary Outcome(s)
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Adverse reaction
[Time Frame: 5 minutes post procedure]
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Secondary ID(s)
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Mhst2014-13
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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