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

NCT01767324 · ClinicalTrials.gov registry record · NA

Site Selection for Intracutaneous Saline Delivery

A NA study, sponsored by FluGen.

Completed
Registry status
NA
Development phase
12
Enrollment target

NCT01767324: Completed NA study, sponsored by FluGen.

NCT01767324 is a NA study that has completed, run by FluGen. The registered enrollment target is 12 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01767324, a NA study, has completed, sponsored by FluGen.

COMPLETED
Registry status
NA
Development phase
12 participants
Enrollment target

Study Summary

The goal of this exploratory study is to select the optimal body site for intracutaneous delivery of 0.5 milliliters of saline from the FLUGEN 101.2 microneedle-based device.

Primary Outcome

Observe injection sites for change of appearance post-dose including wheal formation or resolution.

Interventions

  • DEVICE Injection to deltoid
  • DEVICE Injection to forearm
  • DEVICE Injection to thigh

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2012-12
Est. Completion 2012-12
Phase NA
FluGen

6 total trials

What the finished NCT01767324 record still lists

NCT01767324 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 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 3 interventions - of which Injection to deltoid is the first listed.

NCT01767324 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01767324 about?

NCT01767324 is a clinical study titled "Site Selection for Intracutaneous Saline Delivery". The goal of this exploratory study is to select the optimal body site for intracutaneous delivery of 0.5 milliliters of saline from the FLUGEN 101.2 microneedle-based device.

What is the current status of trial NCT01767324?

This trial is currently completed. It is a NA study. The enrollment target is 12 participants. The study started on 2012-12. Estimated completion is 2012-12.

What interventions are being tested in trial NCT01767324?

The interventions under investigation include: Injection to deltoid (DEVICE), Injection to forearm (DEVICE), Injection to thigh (DEVICE).

Who is sponsoring clinical trial NCT01767324?

This trial is sponsored by FluGen, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01767324's enrollment target sits among peer trials

12 1913th of 2000 higher than 74 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

  • 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 NCT01767324, the US trial registry maintained by the National Library of Medicine. NCT01767324 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.