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Randomized Controlled Trial of TCRFVR and LAUP in Snorers

T

Taichung Veterans General Hospital

Status

Completed

Conditions

Snorer

Treatments

Procedure: TCRFVR and LAUP

Study type

Interventional

Funder types

Other

Identifiers

NCT00202943
TCVGH-917003A
911007

Details and patient eligibility

About

We hypothesis that radiofrequency will cause less post-operative discomfort when compared with laser assited uvulopharyngoplasty. 40 patients with primary snore will be enrolled into this study. After overnight sleep test confimred that no obstructive sleep apnea existed, cases were informed consented. Then they were randomized into two groups. Post-operative pain, duration of analgesics were recorded.

Full description

Although Rf group was less effective, they felt less discomfort.

Sex

All

Ages

20+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • RDI < 5/h

Exclusion criteria

  • Previous treated snoring, coagulation disorder

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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