Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06150469

Efficacy of Inhaled Aromatherapy on Nausea and Vomiting in Hematological Malignancies

Led by University Hospital, Limoges · Updated on 2024-12-12

286

Participants Needed

4

Research Sites

139 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This project will optimise the management of chemotherapy-induced nausea and vomiting, with improvements in nausea and vomiting scores, quality of life and appetite expected in participants benefiting from the intervention. In all cases, the use of complementary methods is recommended and improves the management of people with cancer because they offer a person-centred approach.

CONDITIONS

Official Title

Efficacy of Inhaled Aromatherapy on Nausea and Vomiting in Hematological Malignancies

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged over 18 years
  • Chemo-naive patients at inclusion
  • Patients with haematological malignancies treated with chemotherapy
  • Patients physically and mentally able to use the aromastick
  • Patients who speak, read and write French
  • Patients who have given signed consent
  • Patients with social security cover
Not Eligible

You will not qualify if you...

  • Asthmatic patients
  • Patients with anosmia
  • Patients allergic to essential oils, lemon, or ginger
  • Patients who have already received aromatherapy to treat chemotherapy-induced nausea and vomiting
  • Patients practising herbal medicine or acupuncture
  • Pregnant and breast-feeding women
  • Patients under guardianship, tutorship or curatorship
  • Patients taking part in interventional studies involving antiemetic drugs or nutritional products
  • Patients who have already had cancer

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

CH BRIVE

Brivé, France, 19100

Actively Recruiting

2

Chu La Reunion

La Réunion, France, 97448

Actively Recruiting

3

University Hospital, Limoges

Limoges, France, 87042

Actively Recruiting

4

Ch Poissy

Saint-Germain-en-Laye, France, 78100

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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