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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04325113
Other study ID # Tonsilstopic
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 7, 2019
Est. completion date January 15, 2020

Study information

Verified date March 2020
Source University of Liege
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Check analgesia after tonsillectomy in adults


Description:

We hypothesize that a vaporization of local anesthetics in the tonsil lodge would reduce postoperative pain.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date January 15, 2020
Est. primary completion date December 31, 2019
Accepts healthy volunteers No
Gender All
Age group 14 Years and older
Eligibility Inclusion Criteria:

- Tonsillectomy

Exclusion Criteria:

- Gastric or duodenal ulcer

- Diabetes

- Kidney failure

- Chronic pain and fibromyalgia

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
levobupivacaine
Patient satisfaction and pain score using a visual anagogic scale (VAS)

Locations

Country Name City State
Belgium Javillier Liège

Sponsors (1)

Lead Sponsor Collaborator
University of Liege

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient's satisfaction and pain score patient satisfaction and pain score using a visual anagogic scale from 0 (no pain) to 10 (intolerable pain) until 10 days after the tonsillectomy.
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