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Treatment of Post Operative Pain in Thyroid Surgery Patients: Perspective Study Acupuncture Versus Drugs

The Treatment of Post Operative Pain in Thyroid Surgery Patients: Perspective Study Acupuncture Versus Pharmacological Treatment

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01579786
Enrollment
121
Registered
2012-04-18
Start date
2011-05-31
Completion date
2014-02-28
Last updated
2014-02-20

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

Conditions

Post Operative Pain

Keywords

post operative pain, acupuncture

Brief summary

The aim of the study was to evaluate if acupuncture may reduce intraoperative ULTIVA (remifentanil) consumption and post operative pain measured with VAS, italian version Mc Gill Questionnaire Pain and drug consumption (acetaminophen daily consumption).

Detailed description

The aim of the study was to evaluate if acupuncture may reduce intraoperative ULTIVA (remifentanil) consumption and post operative pain measured with VAS, italian version Mc Gill Questionnaire Pain and drug consumption (acetaminophen daily consumption). The study involve patients who underwent thyroid surgery randomised in two groups. A group patients treated with drugs and B group patients treated with drugs and acupuncture.Acupuncture related risk are pain, faint and haematoma.The study will be done in Padova University Hospital (Endocrine Unit.Primary end point will be VAS pain and secondary end points ULTIVA consumption, post operative pain measured with italian version of Mc Gill Questionnaire Pain and acetaminophen daily intake

Interventions

PROCEDUREAcetaminophen and acupuncture

All patients will receive acetaminophen (maximum 3g/day) for all seven days after surgery and will receive acupuncture treatment at first day after performing surgery and thirty minutes before operation

Sponsors

University of Padova
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* thyroid surgery patients

Exclusion criteria

* back severe arthritis * osteoporosis * myofascial pain * rheumatic disease * fibromyalgia * systemic cardiovascular and respiratory disease * hypertension * drug or alcohol consumption * mental disease * cervical trauma * chronic use of antidepressant * hypnotic and antihypertensive drugs

Design outcomes

Primary

MeasureTime frameDescription
Visual Analogue Scalewithin the 3rd postoperative dayChange in intensity of pain from first day after operation and during the seven days after performing surgery

Secondary

MeasureTime frameDescription
Mc Gill Questionnaire painwithin the 3rd postoperative dayChange in intensity of pain from the day after operation and during all seven days after performing surgery

Other

MeasureTime frame
Remifentanil consumptionIntraoperative
Acetaminophenwithin 7 days after surgery

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026