Pain Induced by m-Cresol as Preservative

Trial statusNot yet recruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-70
SponsorMedical University of Vienna

About this trial

Preservatives such as m-Cresol are essential components in many subcutaneously injected medications, including insulin or human growth hormone, to prevent bacterial growth. However, clinical reports have suggested that these preservatives may cause local discomfort or pain at the injection site, which can negatively impact treatment adherence. While m-Cresol is widely used, its direct contribution to injection-site pain has not yet been investigated in a prospective clinical trial.

This study aims to investigate whether subcutaneous injection of m-Cresol at concentrations commonly used in clinical practice (0.1% and 0.25%) cause significantly more pain than a preservative-free control solution. In a randomized, double-blind crossover design, healthy volunteers will receive three separate injections in a belly fold. Participants will rate their pain every 5 seconds until it subsides. The findings will help determine if m-Cresol is a primary source of injection-site pain and could lead to the development of more comfortable drug formulations.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age between 18 and 70 years

Full legal capacity

Disqualifiers

Participant of another study, ongoing or within the last four weeks

Current medication intake (except hormonal contraception) or drug abuse

Female subjects: Positive pregnancy test or breastfeeding

Body temperature above 38°C, verified by infrared thermometer

Trial design

Design model

Crossover

Treatments tested in this trial

  • m-Cresol 0.1%

    Other intervention

    A preservative administered subcutaneously at 0.1%, a common concentration used in medicines.

  • m-Cresol 0.25%

    Other intervention

    A preservative administered subcutaneously at 0.25%, a common concentration used in medicines.

  • Control Solution

    Other intervention

    A control solution administered subcutaneously.

Treatment groups

18 Participants
are divided into 3 treatment groups
Group A: m-Cresol 0.1%Experimental treatment 1 intervention
Group B: m-Cresol 0.25%Experimental treatment 1 intervention
Group C: Control solutionPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Area Under the Curve (AUC) of Pain Intensity

Total pain burden calculated as the Area Under the Curve of serial pain ratings (0-100 numerical pain rating scale) recorded every 5 seconds from the start of injection until no pain is reported for 30 seconds.

Time frame
From injection start until pain subsides (approximately 15-60 seconds per injection).

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: