Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT03881891 · ClinicalTrials.gov registry record · NA
Optimizing Acute Post-Operative Dental Pain Management Using New Health Information Technology
A NA study, sponsored by University of California, San Francisco.
- Completed
- Registry status
- NA
- Development phase
- 1,525
- Enrollment target
NCT03881891: Completed NA study, sponsored by University of California, San Francisco.
NCT03881891 is a NA study that has completed, run by University of California, San Francisco. The registered enrollment target is 1,525 participants, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03881891, a NA study, has completed, sponsored by University of California, San Francisco.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,525 participants
- Enrollment target
Study Summary
The investigators seek to implement a dental patient reported outcomes system using mobile phone and text messaging to target the over-reliance on pre-emptively prescribed opioids by dental providers. If successful, this project will help dentists actively track and manage their patients' pain after hours and enhance the overall care experience.
Primary Outcome
Evaluate the pain intensity on Day 1 following completion of the specified dental procedures. Raw scores for the pain intensity construct are determined by summing each of the individual scores from the three questions for each participant. The raw scores are then standardized using a T-score, which ranges from 0 to 100 with a mean of 50 and standard deviation of 10. Scores closer to 100 indicate high pain intensities and scores closer to 0 indicate lower pain intensities.
Interventions
- BEHAVIORAL Follow-app intervention arm
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,525 participants |
| Start Date | 2020-02-03 |
| Est. Completion | 2022-06-30 |
| Phase | NA |
What the finished NCT03881891 record still lists
NCT03881891 is an interventional study that assigns participants to a tested intervention. Its 1,525 participants enrollment target places it among the larger protocols in the corpus, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target.
The record links to 0 conditions, and to 1 intervention - of which Follow-app intervention arm is the first listed.
NCT03881891 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03881891 about?
NCT03881891 is a clinical study titled "Optimizing Acute Post-Operative Dental Pain Management Using New Health Information Technology". The investigators seek to implement a dental patient reported outcomes system using mobile phone and text messaging to target the over-reliance on pre-emptively prescribed opioids by dental providers. If successful, this project will help dentists actively track and manage their patients' pain after...
What is the current status of trial NCT03881891?
This trial is currently completed. It is a NA study. The enrollment target is 1,525 participants. The study started on 2020-02-03. Estimated completion is 2022-06-30.
What interventions are being tested in trial NCT03881891?
The interventions under investigation include: Follow-app intervention arm (BEHAVIORAL).
Who is sponsoring clinical trial NCT03881891?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03881891's enrollment target sits among peer trials
1,525 65th of 2000 higher than 1,936 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
- NCT06257082 · 1,526 participants · NA
Video-based Patient Education Intervention for Diabetic Eye Screening in Latinx Communities
- NCT06876714 · 1,524 participants · Phase 3
ShortStop-HER2: 12 Months vs. 6 Months of HER2-targeted Medications for People With HER2+ Breast Cancer Who Had a Pathologic Complete Response After Chemotherapy Plus Trastuzumab
- NCT06623097 · 1,528 participants · NA
Exercise and Nutrition for Older Cancer Survivors and Their Support Person: The Vitality Study
- NCT06393374 · 1,530 participants · Phase 3
Sacituzumab Tirumotecan (MK-2870) Plus Pembrolizumab Versus TPC in TNBC Who Did Not Achieve pCR (MK-2870-012)
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