A Trial Investigating the Influence of Injection Speed and Volume on the Perception of Subcutaneous Injection Pain

Status

Completed

Phases

Phase 1

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01937702

Enrollment

Registered

2013-09-09

Start date

2014-04-30

Completion date

2014-09-30

Last updated

2014-12-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus

Brief summary

A trial, investigating the influence of injection speed and volume on the perception of subcutaneous injection pain.

Interventions

OTHER0.9% NaCl (sodium chloride)

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

BASIC_SCIENCE

Masking

DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender

ALL

Age

18 Years to 74 Years

Healthy volunteers

Inclusion criteria

* Subject has signed the informed consent form prior to screening * Age 18-74 years at screening (both included)

Exclusion criteria

* Known or suspected hypersensitivity to needle, ink ball pen or other that are in contact with the injection area during the clinical visit * Previous participation in this trial. Participation is defined as having received at least one injection

Design outcomes

Primary

Measure	Time frame
injection pain	within 24 hours after injection

Secondary

Measure	Time frame
variability of injection pain	within the first 24 hours after injection

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026