Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04187950 · ClinicalTrials.gov registry record · NA

NECTAR Study: Nectar (Honey) Effects on Comfort, Thoughts, and Regularity

A NA study of Physiological Stress and Gastrointestinal Dysfunction, sponsored by University of Illinois at Urbana-Champaign.

Completed
Registry status
NA
Development phase
66
Enrollment target
1
Study location

NCT04187950: Completed NA study of Physiological Stress and Gastrointestinal Dysfunction, sponsored by University of Illinois at Urbana-Champaign.

NCT04187950 is a NA study of Physiological Stress and Gastrointestinal Dysfunction that has completed, run by University of Illinois at Urbana-Champaign. The registered enrollment target is 66 participants, roughly in line with the 62-participant average among 6 other Physiological Stress trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04187950, a NA study of Physiological Stress and Gastrointestinal Dysfunction, has completed, sponsored by University of Illinois at Urbana-Champaign.

COMPLETED
Registry status
NA
Development phase
66 participants
Enrollment target
1
Study location

Study Summary

This study aims to test the central hypothesis that adding to the diet daily yogurt with honey provides beneficial effects on digestive health and subjective mood in healthy adults.

Primary Outcome

Determine the impact of consumption of daily yogurt with honey on intestinal transit time in vivo compared to control, yogurt containing heat-inactivated B.lactis with added sugar. Intestinal transit time will be measured using colored dye markers.

Interventions

  • DIETARY_SUPPLEMENT Yogurt with B. lactis and added honey
  • DIETARY_SUPPLEMENT Yogurt with heat-inactivated B. lactis and added cane sugar

Study Locations (1)

Illinois

  • University of Illinois at Urbana-Champaign - Urbana

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2021-05-19
Est. Completion 2022-11-02
Phase NA

What the finished NCT04187950 record still lists

NCT04187950 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 66 participants, a relatively small participant target, roughly in line with the 62-participant average among 6 other Physiological Stress trials with a reported enrollment target.

The record links to 3 conditions, with Physiological Stress appearing as the primary indexed condition, and to 2 interventions - of which Yogurt with B. lactis and added honey is the first listed.

NCT04187950 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT04187950 about?

NCT04187950 is a clinical study titled "NECTAR Study: Nectar (Honey) Effects on Comfort, Thoughts, and Regularity". This study aims to test the central hypothesis that adding to the diet daily yogurt with honey provides beneficial effects on digestive health and subjective mood in healthy adults.

What is the current status of trial NCT04187950?

This trial is currently completed. It is a NA study. The enrollment target is 66 participants. The study started on 2021-05-19. Estimated completion is 2022-11-02.

What conditions does trial NCT04187950 study?

This clinical trial studies the following conditions: Physiological Stress, Gastrointestinal Dysfunction, Cognition - Other.

What interventions are being tested in trial NCT04187950?

The interventions under investigation include: Yogurt with B. lactis and added honey (DIETARY_SUPPLEMENT), Yogurt with heat-inactivated B. lactis and added cane sugar (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT04187950?

This trial is sponsored by University of Illinois at Urbana-Champaign, which has 129 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04187950 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Physiological Stress

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02584244 · 66 participants · Phase 1

    Feasibility of the LUM Imaging System for Detection of Gastrointestinal Cancers

  • NCT03067051 · 66 participants · Phase 1

    Clinical Study to Assess the Safety and Efficacy of the SpectraCure P18 System

  • NCT03754725 · 66 participants · Phase 1

    Ferritin and Iron Burden in SAH sIRB

  • NCT03875378 · 66 participants · Phase 2

    Transdermal Estrogen in Women With Anorexia Nervosa

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04187950, the US trial registry maintained by the National Library of Medicine. NCT04187950 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.