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Acupuncture for Recovery and Postoperative Nausea and Vomiting After Middle Ear Surgeries

Acupuncture for Enhancing Recovery and Attenuating Postoperative Nausea and Vomiting After Middle Ear Surgeries: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04748133
Enrollment
59
Registered
2021-02-10
Start date
2021-02-20
Completion date
2021-07-01
Last updated
2021-02-24

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

Conditions

Treatment Complication

Brief summary

Modern surgery management needs increasing operating room turnover and more ambulatory surgery. In order to come over this challenge, the recovery needs to be optimized. Enhancing recovery could be achieved by preventing postoperative pain and postoperative nausea and vomiting. Middle ear surgery is a common ambulatory surgery with increasing occurrence of postoperative nausea and vomiting.

Detailed description

Sample size: as percent of vomiting following acupuncture and following standard anesthesia is 0.13% and 29.2% respectively so sample size is 58 (29 in each group). Sample is calculated using open epi program with confidence level 95% and power 80%. Patients in Group C (control group) (n=29): will receive no treatment. While patients in Group A (Acupuncture group) (n=29): will receive needle acupuncture.

Interventions

Site of acupuncture points: * Du 26: At junction of the upper and middle third of philtrum. * Ren 17: On the midline level with the 4th intercostal space midway between the nipples. * LI4 (Large Intestine 4): On the dorsum of the hand, between the 1st and 2nd metacarpal bones * HT7 (Heart 7): On the ulnar end of the transverse crease of the wrist, in the small depression between the pisiform and ulna bones * LV3 (Liver 3): On dorsum of the foot in a depression distal to the junction of the 1st and 2nd metatarsal bones. * ST36 (Stomach 36): Antero-lateral leg, 1 middle-finger breadth next to the anterior crest of tibia, 3 cun under the depression lateral to the patellar ligament. * PC6 (Pericardium 6): Palmar aspect of the forearm, between the tendons, 2 cun away from the transverse crease of the wrist

OTHERplacebo

no treatment

Sponsors

Zagazig University
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
21 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Written informed consent from the patient. * Age: 21-60 years old. * Sex: both sex (males or females). * Physical status: ASA 1& II. * BMI = (20-30 kg/m2). * Type of operations: elective unilateral middle ear surgeries such as tempanoplasty, stapedectomy and mastedictomy.

Exclusion criteria

* Altered mental state * Patients with Drug abuse or alcohol. * Patients with on antipsychotic drugs, regular antiemetic therapy or receiving antiemetic 24 hour before surgery. * Patients with pre-treatment with acupuncture or trigger point injection. * Pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
incidence of postoperative nausea and vomitingup to 24 hours postoperativePostoperative nausea and vomiting impact scale score . Questions Answers score Did you have vomiting or dry retching? No 0 Once 1 Twice 2 Three or more times 3 Have you experienced a feeling of nausea? If yes, has it interfered with your daily activities? Not at all 0 Sometimes 1 Often/most of the times 2 All the time 3 Summation of numerical answer to question 1 plus 2 equal the PONV impact scale. PONV Impact Scale Score of ≥5 represents clinically important PONV

Secondary

MeasureTime frameDescription
recovery timeup to 30 minutes postoperativetime from discontinuation of isoflurane to first response to verbal command
The time of dischargeup to 30 minutes postoperativeThe time from arrival to PACU to discharge to the ward) according to Modified Aldert score Modified Aldert score . Assessment item Condition Grade Activity, able to move, voluntarily or on command 4 extremities 2 2 extremities 1 No 0 Breathing Able to breathe deeply & cough freely 2 Dyspnea, shallow or limited breathing 1 Apnea 0 Consciousness Fully awake 2 Arousable on calling 1 Unresponsive 0 Circulation (blood pressure) ±20% of pre-anesthesia level 2 * 20% to 49% of pre-anesthesia level 1 * 50% of pre-anesthesia level 0 SPO2 Maintain SPO2 \>92% in ambient air 2 Maintain SPO2 \>90% with O2 1 Maintain SPO2 \<90% with O2 0 Patient having a score of 9 or higher is discharged
extubation timeup to 10 minutes postoperativetime from discontinuation of isoflurane to extubation
Postoperative Painup to 30 minutes, 2 hours and 4 hours postoperativeVisual Analogue Scale (VAS) . A commonly used scale is a 10-cm line labeled with worst pain imaginable on the right border and no pain on the left border. The patient is instructed to make a mark along the line to represent the intensity of pain currently being experienced. IV paracetamol 1 gm every 6hs as a protocol for pain management and IV pethidine 30 mg as rescue analgesic will be given if VAS ≥ 4. Total doses and number of analgesics will be recorded
number of participant with side effects of acupunctureup to 24 hours postoperativebleeding, soreness, or bruising at the site of needle insertion
The total number of rescue antiemetic (metoclopramide)in the first 24 hour postoperativeAny patient will receive 10 mg intravenous metoclopramide immediately if there is nausea and vomiting

Countries

Egypt

Contacts

Primary ContactMarwa Zakzouk, MD
dr.marwa.zu@gmail.com01004178761
Backup ContactAl shaimaa Kamel, MD
AlshaimaaKamel80@yahoo.com01005593169

Outcome results

None listed

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