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

NCT06965803 · ClinicalTrials.gov registry record

This Study is to Evaluate Whether Receiving Education and Glucose Monitoring With the CGM Device Will Improve Patient-reported Outcomes by Improving Patient's Satisfaction and Quality of Life (QOL) With Glucose Monitoring Device

A clinical trial of Diabetes Mellitus, sponsored by Cedars-Sinai Medical Center.

Recruiting
Registry status
37
Enrollment target
1
Study location

NCT06965803: Recruiting study of Diabetes Mellitus, sponsored by Cedars-Sinai Medical Center.

NCT06965803 is a study of Diabetes Mellitus that is actively recruiting participants, run by Cedars-Sinai Medical Center. The registered enrollment target is 37 participants, below the 1,867-participant average among 208 other Diabetes Mellitus trials with a reported enrollment target (98% lower). 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

NCT06965803, a study of Diabetes Mellitus, is actively recruiting participants, sponsored by Cedars-Sinai Medical Center.

RECRUITING
Registry status
37 participants
Enrollment target
1
Study location

Study Summary

The purpose of the study is to improve patient-reported outcomes by improving patient's satisfaction and quality of life (QOL) with glucose monitoring device through pre and post satisfaction survey of patient with diabetes.

Primary Outcome

Glucose Monitoring Satisfaction Survey

Conditions Studied

Study Locations (1)

California

  • Cedars-Sina Medical Center - Los Angeles

Trial Details

FieldValue
Enrollment Target 37 participants
Start Date 2025-10-01
Est. Completion 2026-12-30
Cedars-Sinai Medical Center

339 total trials

What NCT06965803 shows while recruiting

NCT06965803 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 37 participants, a relatively small participant target, below the 1,867-participant average among 208 other Diabetes Mellitus trials with a reported enrollment target (98% lower).

The record links to 1 condition, with Diabetes Mellitus appearing as the primary indexed condition, and to 0 interventions.

NCT06965803 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT06965803 about?

NCT06965803 is a clinical study titled "This Study is to Evaluate Whether Receiving Education and Glucose Monitoring With the CGM Device Will Improve Patient-reported Outcomes by Improving Patient's Satisfaction and Quality of Life (QOL) With Glucose Monitoring Device". The purpose of the study is to improve patient-reported outcomes by improving patient's satisfaction and quality of life (QOL) with glucose monitoring device through pre and post satisfaction survey of patient with diabetes.

What is the current status of trial NCT06965803?

This trial is currently recruiting. The enrollment target is 37 participants. The study started on 2025-10-01. Estimated completion is 2026-12-30.

What conditions does trial NCT06965803 study?

This clinical trial studies the following conditions: Diabetes Mellitus.

Who is sponsoring clinical trial NCT06965803?

This trial is sponsored by Cedars-Sinai Medical Center, which has 339 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06965803 being conducted?

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

Similar trials for Diabetes Mellitus

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.

Where NCT06965803's enrollment target sits among peer trials

37 170th of 208 higher than 37 of 208 other Diabetes Mellitus trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Diabetes Mellitus 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

  • NCT02800486 · 37 participants · Phase 2

    Super Selective Intra-arterial Repeated Infusion of Cetuximab (Erbitux) With Reirradiation for Treatment of Relapsed/Refractory GBM, AA, and AOA

  • NCT03173937 · 37 participants · Phase 1

    Unrelated Umbilical Cord Blood Transplantation for Severe Aplastic Anemia and Hypo-plastic MDS Using CordIn(TM), Umbilical Cord Blood-Derived Ex Vivo Expanded Stem and Progenitor Cells to Expedite Engraftment and Improve Transplant Outcome

  • NCT03295227 · 37 participants · Phase 1

    Pembrolizumab in Treating Participants With Unresectable Thymoma or Thymic Cancer

  • NCT03401047 · 37 participants · Early Phase 1

    Study to Assess Potential Impairments in Estradiol Augmentation of Gonadotropin Secretion in Polycystic Ovary Syndrome

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 NCT06965803, the US trial registry maintained by the National Library of Medicine. NCT06965803 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.