← Back to Clinical Trials
Recruiting NCT07201194

NCT07201194 Holistic Acupuncture for Patients With Chemotherapy Induced Nausea

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07201194
Status Recruiting
Phase
Sponsor Vejle Hospital
Condition Breast Cancer
Study Type INTERVENTIONAL
Enrollment 90 participants
Start Date 2025-11-17
Primary Completion 2027-04

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Holistic acupuncture and acupressureStandard medical treatment

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 90 participants in total. It began in 2025-11-17 with a primary completion date of 2027-04.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The study explores whether acupuncture as a supplement to conventional antiemetic medicine is superior in reducing the level of chemotherapy induced nausea compared to conventional anitemetic medicine alone. A total of 90 patients experiencing chemotherapy induced nausea will be allocated 1:1 to either acupuncture and antiemetic medicine or antiemetic medicine alone. The level of nausea and other cancer related symptoms will be assessed at baseline and 8 and 22 days after enrollment

Eligibility Criteria

Inclusion criteria * ≥ 18 years of age * Undergoing chemotherapy and experiencing nausea despite adherence to the prescribed antiemetic regimen * Understands and speaks Danish * Written and orally informed consent * Planned for treatment every 14 days * At least two chemotherapy cycles planned at the time of inclusion Exclusion Criteria: * Brain metastases * Performance status \>2

Contact & Investigator

Central Contact

Mette Stie, PhD

✉ mette.stie@rsyd.dk

📞 +4579409174

Principal Investigator

Mette Stie, Phd

PRINCIPAL INVESTIGATOR

Department of Oncology, Lillebaelt Hospital, Vejle

Frequently Asked Questions

Who can join the NCT07201194 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Breast Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07201194 currently recruiting?

Yes, NCT07201194 is actively recruiting participants. Contact the research team at mette.stie@rsyd.dk for enrollment information.

Where is the NCT07201194 trial being conducted?

This trial is being conducted at Vejle, Denmark.

Who is sponsoring the NCT07201194 clinical trial?

NCT07201194 is sponsored by Vejle Hospital. The principal investigator is Mette Stie, Phd at Department of Oncology, Lillebaelt Hospital, Vejle. The trial plans to enroll 90 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology