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

NCT01369680 · ClinicalTrials.gov registry record · Phase 1

Oral Ketamine for Control of Chronic Pain in Children

A Phase 1 study of Chronic Pain, sponsored by University of Rochester.

Completed
Registry status
Phase 1
Development phase
12
Enrollment target
1
Study location

NCT01369680: Completed Phase 1 study of Chronic Pain, sponsored by University of Rochester.

NCT01369680 is a Phase 1 study of Chronic Pain that has completed, run by University of Rochester. The registered enrollment target is 12 participants, below the 772-participant average among 301 other Chronic Pain 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

NCT01369680, a Phase 1 study of Chronic Pain, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
Phase 1
Development phase
12 participants
Enrollment target
1
Study location

Study Summary

The study is a maximum tolerated dose finding study for oral, chronic, daily administration of oral ketamine (by mouth) in children with long-term daily pain.

Primary Outcome

According to CTCae any dose causing grade 2 or worse toxicity will be an untolerated dose. Tolerability is defined as ability to take the medication for 2 weeks without having a grade 2 or worse toxicity.

Conditions Studied

Interventions

  • DRUG Ketamine

Study Locations (1)

New York

  • University of Rochester - Rochester

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2011-05
Est. Completion 2012-10
Phase Phase 1
University of Rochester

636 total trials

What the finished NCT01369680 record still lists

NCT01369680 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 772-participant average among 301 other Chronic Pain trials with a reported enrollment target (98% lower).

The record links to 1 condition, with Chronic Pain appearing as the primary indexed condition, and to 1 intervention - of which Ketamine is the first listed.

NCT01369680 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT01369680 about?

NCT01369680 is a clinical study titled "Oral Ketamine for Control of Chronic Pain in Children". The study is a maximum tolerated dose finding study for oral, chronic, daily administration of oral ketamine (by mouth) in children with long-term daily pain.

What is the current status of trial NCT01369680?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2011-05. Estimated completion is 2012-10.

What conditions does trial NCT01369680 study?

This clinical trial studies the following conditions: Chronic Pain.

What interventions are being tested in trial NCT01369680?

The interventions under investigation include: Ketamine (DRUG).

Who is sponsoring clinical trial NCT01369680?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01369680 being conducted?

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

Similar trials for Chronic Pain

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 NCT01369680's enrollment target sits among peer trials

12 287th of 301 higher than 13 of 301 other Chronic Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Chronic Pain 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

  • NCT02602769 · 12 participants

    Whole Transcriptome Profiling and Metabolic Phenotyping in Children With ROHHAD Syndrome

  • NCT02605421 · 12 participants · Phase 2

    Myeloablative Consolidation Therapy and Tandem Autologous Stem Cell Rescue in Patients With High-Risk Neuroblastoma

  • NCT02619448 · 12 participants · Early Phase 1

    Concurrent Chemotherapy Plus HFR Radiation Therapy in Inoperable NSCLC

  • NCT03311503 · 12 participants · Phase 1

    Phase I/II Trial of Lentiviral Gene Transfer for SCID-X1 With Low Dose Targeted Busulfan Conditioning

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01369680, the US trial registry maintained by the National Library of Medicine. NCT01369680 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.