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Acupuncture in the care of nausea and vomiting after surgery

The use of acupuncture in the prevention of nausea and vomiting postoperative

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9kwjgx
Enrollment
Unknown
Registered
2017-04-17
Start date
2016-10-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

nausea and vomiting postoperative.

Interventions

There will be two groups of 33 patients each. Intervention group: Collection 2 ml blood, acupuncture application with bilateral needle P6 points (Neiguam) PACU, lasting 30 minutes, new blood collecti
Procedure/surgery
Other
C23.550.767.859

Sponsors

Departamento de Anestesiologia da Faculdade de Medicina da Universidade Estadual Paulista
Lead Sponsor
Faculdade de Medicina da Universidade Estadual Paulista
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: female patients , aged 18 to 65 years , physical status I and II according to the American Society of Anesthesiologists ( ASA ) , undergoing abdominal elective gynecological surgery ( hysterectomy) under total intravenous anesthesia.

Exclusion criteria

Exclusion criteria: patients under 18 years , ASA III or IV , unable to report or respond to protocol , fear of acupuncture needle , inability to use P6 ( Neiguam ) , patients using a different antiemetic protocol .

Design outcomes

Primary

MeasureTime frame
For the quantitative variables will be held the variance analysis in a completely randomized design . For qualitative variables will be held Fisher's exact test . The level of significance will be 5% . * It will be assessed the frequency of nausea and vomiting in both groups up to 24 h after surgery. * Plasma serotonin and dopamine will be quantified before and after acupuncture and acupressure group without also in order to see if acupuncture interfere plasma levels of these . For the quantitative variables will be held the variance analysis in a completely randomized design. For qualitative variables will be held Fisher's exact test. The level of significance will be 5%.

Secondary

MeasureTime frame
dont have

Countries

Brazil

Contacts

Public ContactMichelle Pires

Departamento de Anestesiologia - Faculdade de medicina de Botucatu - Universidade Estadual Paulista

catarinamcatarinap@gmail.com+55 (14) 38801407

Outcome results

None listed

Source: REBEC (via WHO ICTRP)