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Recruiting NCT06189794

NCT06189794 Effects of Rosa Damascena and Frankincense Essential Oils in Labor

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Clinical Trial Summary
NCT ID NCT06189794
Status Recruiting
Phase
Sponsor Balikesir University
Condition Labor Pain
Study Type INTERVENTIONAL
Enrollment 39 participants
Start Date 2024-01-21
Primary Completion 2025-12-21

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 49 Years
Study Type INTERVENTIONAL
Interventions
Rosa damascena oil

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 39 participants in total. It began in 2024-01-21 with a primary completion date of 2025-12-21.

⚠ 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

This randomized controlled study aims to compare effects of different essential oils in labor pain, anxiety and childbirth comfort. The main questions it aims to answer are: Is it effective using rosa damascena oil during labor? Is it effective using frankincense oil during labor? Which essential oil is more effective during labor Researchers will compare aromatherapy oils groups to see labor pain, anxiety and childbirth comfort levels of pregnant women.

Eligibility Criteria

Inclusion Criteria: \- Pregnant women who are at latent phase of labor Exclusion Criteria: * Complicated pregnancy (preeclampsia, hypertension, diabetes etc.) * Women who will have planned cesarean section * Asthma or any other respiratory disease * Allergies to Rosa Damascena or Frankincense oil

Contact & Investigator

Central Contact

Tuba Kızılkaya, Asst.Prof.

✉ kizilkaya.tb@gmail.com

📞 +905514051804

Principal Investigator

Tuba Kızılkaya, Asst.Prof.

PRINCIPAL INVESTIGATOR

Balikesir University Hospital

Frequently Asked Questions

Who can join the NCT06189794 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 49 Years, studying Labor Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06189794 currently recruiting?

Yes, NCT06189794 is actively recruiting participants. Contact the research team at kizilkaya.tb@gmail.com for enrollment information.

Where is the NCT06189794 trial being conducted?

This trial is being conducted at Balıkesir, Turkey (Türkiye).

Who is sponsoring the NCT06189794 clinical trial?

NCT06189794 is sponsored by Balikesir University. The principal investigator is Tuba Kızılkaya, Asst.Prof. at Balikesir University Hospital. The trial plans to enroll 39 participants.

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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