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Auriculotherapy for Prevention of Postoperative Urinary Retention

Auriculotherapy for Prevention of Postoperative Urinary Retention in Men Receiving Postoperative Epidural Analgesia After Thoracic Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02290054
Acronym
RUPO
Enrollment
53
Registered
2014-11-13
Start date
2014-04-30
Completion date
2016-05-23
Last updated
2017-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Analgesia, Epidural

Keywords

analgesia, epidural, urinary retention

Brief summary

Urinary retention is a common complication of epidural analgesia. Auriculotherapy could prevent this complication. This study will be performed among men receiving thoracic epidural analgesia after thoracic surgery.

Interventions

PROCEDUREControl

Implementation of adhesive pads on the ears is performed while the patient is sleeping but before thoracic incision.

PROCEDURETreated

Auriculotherapy uses semi-permanent needles and implementation of adhesive pads to mask the needles.

PROCEDUREIntra-venous anesthesia

Sponsors

Hopital Foch
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* patients scheduled to a lung surgical procedure and thoracic epidural analgesia

Exclusion criteria

* Abnormalities of the external ear * Dialysis or end stage renal failure * Abnormal urinary tract * Incapacity to self assessment of comfort and anxiety, * Contra-indication to total intravenous anesthesia

Design outcomes

Primary

MeasureTime frameDescription
bladder catheterization24 hoursRequirement of bladder catheterization during the day and the first night following surgery

Secondary

MeasureTime frameDescription
Comfort24 hoursThe degree of patient's comfort is assessed six hours after his arrival in the recovery room and the morning after surgery using a numerical scale from 0 'maximum discomfort to 10 maximum comfort
Anxiety24 hoursThe degree of patient's anxiety is assessed six hours after his arrival in the recovery room and the morning after surgery using a numerical scale from 0 'maximum discomfort to 10 maximum comfort

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026