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NCT03513536 · ClinicalTrials.gov registry record · NA

The Effect of Scent on Pregnancy Induced Nausea, Vomiting, and Quality of Life

A NA study, sponsored by Nutraceuticals Research Institute.

Completed
Registry status
NA
Development phase
74
Enrollment target

NCT03513536: Completed NA study, sponsored by Nutraceuticals Research Institute.

NCT03513536 is a NA study that has completed, run by Nutraceuticals Research Institute. The registered enrollment target is 74 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03513536, a NA study, has completed, sponsored by Nutraceuticals Research Institute.

COMPLETED
Registry status
NA
Development phase
74 participants
Enrollment target

Study Summary

This study evaluates the effects of essential oils on nausea, vomiting, and quality of life scores among pregnant women. Participants will receive either an essential oil roll-on product or a placebo product to apply to their temples and jaw line daily for 6 days.

Primary Outcome

Nausea and vomiting are measured once per day using the 6-item Quantification of Emesis 24-hour scale (PUQE) scale. This scale includes 3 questions which are ranked on a scale of 1-5, with higher scores indicating higher levels of pregnancy-induced nausea and vomiting. The other 3 questions are open-ended questions which ask participants about perceived well-being.

Interventions

  • OTHER Control
  • OTHER Citrus-Based Aromatherapy
  • OTHER Mint-Based Aromatherapy
  • OTHER Spice-Scented Aromatherapy

Trial Details

FieldValue
Enrollment Target 74 participants
Start Date 2018-04-15
Est. Completion 2020-03-29
Phase NA
Nutraceuticals Research Institute

15 total trials

What the finished NCT03513536 record still lists

NCT03513536 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 4 interventions - of which Control is the first listed.

NCT03513536 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03513536 about?

NCT03513536 is a clinical study titled "The Effect of Scent on Pregnancy Induced Nausea, Vomiting, and Quality of Life". This study evaluates the effects of essential oils on nausea, vomiting, and quality of life scores among pregnant women. Participants will receive either an essential oil roll-on product or a placebo product to apply to their temples and jaw line daily for 6 days.

What is the current status of trial NCT03513536?

This trial is currently completed. It is a NA study. The enrollment target is 74 participants. The study started on 2018-04-15. Estimated completion is 2020-03-29.

What interventions are being tested in trial NCT03513536?

The interventions under investigation include: Control (OTHER), Citrus-Based Aromatherapy (OTHER), Mint-Based Aromatherapy (OTHER), Spice-Scented Aromatherapy (OTHER).

Who is sponsoring clinical trial NCT03513536?

This trial is sponsored by Nutraceuticals Research Institute, which has 15 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03513536's enrollment target sits among peer trials

74 1082nd of 2000 higher than 912 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03513536, the US trial registry maintained by the National Library of Medicine. NCT03513536 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.