Anxiety Clinical Trial
— AcuAnxOfficial title:
Auricular Acupuncture vs. Standard Therapy for Treatment of Preoperative Anxiety in Patients Scheduled for Ambulatory Gynaecological Surgery - a Pilot Non-randomized Controlled Trial
In this prospective nonrandomized study the investigators are going to investigate whether
auricular acupuncture with indwelling fixed needles is feasible for treatment of
preoperative anxiety.
Patients, scheduled for ambulatory gynecologic surgery, will be asked, if they wish to
receive auricular acupuncture (AA) against preoperative anxiety. The patients who will not
wish AA, will be asked to take part in questioning (State-Trait-Anxiety-Inventory (STAI)
questionnaire) and will form the control group. The preoperative anxiety using STAI, as well
as the duration and quality of sleep on the night before surgery, the incidence of side
effects, blood pressure and heart rate will be the outcome measures in this study.
| Status | Completed |
| Enrollment | 42 |
| Est. completion date | May 2016 |
| Est. primary completion date | May 2016 |
| Accepts healthy volunteers | No |
| Gender | Female |
| Age group | 19 Years to 55 Years |
| Eligibility |
Inclusion Criteria: 1. Patients with an American Society of Anaesthesiologists physical status of I to II scheduled for elective ambulatory gynaecological surgery under standardized general anaesthesia 2. Surgery time does not exceed 60 minutes 3. Patients without previous opioid and psychotropic medication 4. Patients aged between 19 and 55 years, able to fill in the STAI questionnaire 5. Patients who have given written informed consent Exclusion Criteria: 1. Current psychiatric disease 2. Local skin infection at the sites of acupuncture 3. Aged < 19 or > 55 years 4. Failure to follow the standardized schema of general anaesthesia 5. Surgery time more than 60 minutes 6. Intraoperative complications (bleeding, required blood transfusion more than 6 units of packed cells, cardiovascular instability, required catecholamines) 7. Patients who consumed opioid medication at least 6 months before surgery 8. Patients who are unable to understand the consent form or to fill in the STAI questionnaire |
Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Germany | University Medicine of Greifswald | Greifswald |
| Lead Sponsor | Collaborator |
|---|---|
| University Medicine Greifswald |
Germany,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Situational anxiety_1 | State (situational) anxiety will be measured using State-Trait-Anxiety Inventory (STAI). | Situational anxiety_1 will be measured on the day before surgery before auricular acupuncture | No |
| Primary | Situational anxiety_2 | State (situational) anxiety will be measured using State-Trait-Anxiety Inventory | Situational anxiety_2 will be measured and in the evening of the day before surgery | No |
| Primary | Situational anxiety_3 | State (situational) anxiety will be measured using State-Trait-Anxiety Inventory | Situational anxiety_3 will be measured on the day of surgery immediately before the operation | No |
| Secondary | Heart rate | On the day of surgery before the surgery | Yes | |
| Secondary | Blood pressure | On the day of surgery before the surgery | Yes |
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