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

NCT05963594 · ClinicalTrials.gov registry record · NA

To Evaluate the Post-Prandial Metabolic Effects of Oligomalt in Adults With T2D and in HAO

A NA study, sponsored by Société des Produits Nestlé (SPN).

Completed
Registry status
NA
Development phase
44
Enrollment target

NCT05963594: Completed NA study, sponsored by Société des Produits Nestlé (SPN).

NCT05963594 is a NA study that has completed, run by Société des Produits Nestlé (SPN). The registered enrollment target is 44 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05963594, a NA study, has completed, sponsored by Société des Produits Nestlé (SPN).

COMPLETED
Registry status
NA
Development phase
44 participants
Enrollment target

Study Summary

The goal of this mechanistic, exploratory study is to compare the effectiveness of Oligomalt to Glucidex 40 after eating in adults with Type 2 Diabetes (T2D) and in otherwise healthy adults with overweight or obesity (HAO).

Primary Outcome

Comparisons in the T2D group: 50 g Oligomalt vs 50 g Glucidex 40. Comparisons in the HAO group: 33 g Oligomalt vs 33 g Glucidex 40 and 50 g Oligomalt vs 50 g Glucidex 40.

Interventions

  • DIETARY_SUPPLEMENT maltodextrin
  • DIETARY_SUPPLEMENT Oligomalt

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2023-01-23
Est. Completion 2023-03-28
Phase NA

What the finished NCT05963594 record still lists

NCT05963594 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 2 interventions - of which maltodextrin is the first listed.

NCT05963594 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05963594 about?

NCT05963594 is a clinical study titled "To Evaluate the Post-Prandial Metabolic Effects of Oligomalt in Adults With T2D and in HAO". The goal of this mechanistic, exploratory study is to compare the effectiveness of Oligomalt to Glucidex 40 after eating in adults with Type 2 Diabetes (T2D) and in otherwise healthy adults with overweight or obesity (HAO).

What is the current status of trial NCT05963594?

This trial is currently completed. It is a NA study. The enrollment target is 44 participants. The study started on 2023-01-23. Estimated completion is 2023-03-28.

What interventions are being tested in trial NCT05963594?

The interventions under investigation include: maltodextrin (DIETARY_SUPPLEMENT), Oligomalt (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT05963594?

This trial is sponsored by Société des Produits Nestlé (SPN), which has 53 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05963594's enrollment target sits among peer trials

44 1423rd of 2000 higher than 566 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

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

  • NCT02323945 · 44 participants · NA

    Effects of Breathing Mild Bouts of Low Oxygen on Limb Mobility After Spinal Injury

  • NCT03093909 · 44 participants · Phase 1

    Study of Aerosol Gemcitabine in Patients With Solid Tumors and Pulmonary Metastases

  • NCT03104491 · 44 participants · Phase 1

    Inotuzumab Ozogamicin Post-Transplant For Acute Lymphocytic Leukemia

  • NCT03781765 · 44 participants · Phase 4

    Stimulant vs. Non-stimulant Treatments and Reward Processing in Drug-naive Youth at SUD Risk

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 NCT05963594, the US trial registry maintained by the National Library of Medicine. NCT05963594 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.