Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07261982

Efficacy of Pressure Pad vs Pressure Bandage Immobilisation for Snake Bite First Aid in Healthy Volunteers

Led by Townsville University Hospital · Updated on 2025-12-16

24

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Snake bites affect thousands of people in Australia each year, with few deaths due to timely medical care and quality first aid. This research investigates and compares two first aid methods—the Pressure Bandage Immobilisation (PBI) technique currently recommended in Australia and a simpler Pressure Pad (PP) technique used internationally. The study aims to determine if the PP method is as effective as PBI in slowing venom movement through the body, which is important for improving first aid guidance. Participants will receive an injection of mock venom in the hand or foot, followed by application of either no first aid, the PBI method, or the PP method. Each technique involves specific bandaging and splinting to immobilize the limb, with pressure carefully controlled around 60mmHg. The study will monitor the flow of the mock venom in each case using nuclear medicine imaging to track its movement through the lymphatic system. During the study, participants will undergo repeated scans to observe how quickly the mock venom reaches regional lymph nodes, with each person experiencing all possible combinations of injection site and first aid method in random order. The primary measure is the time taken for the venom to travel to lymph nodes, monitored over a period spanning a minimum of 12 weeks to a maximum of 18 months. This detailed data will help assess the effectiveness and safety of these first aid techniques to inform future recommendations.

CONDITIONS

Brief Title

Analysis of the Efficacy of Pressure Pad vs Pressure Bandage Immobilisation for Snake Bite First Aid in Healthy Volunteers.

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years old or greater
  • No known or clinically evident lymphatic condition such as lymphoedema or lymph node surgery
  • No known cardiac failure
  • No known peripheral vascular disease
  • No known renal or hepatic impairment
  • No known lymphoma
Not Eligible

You will not qualify if you...

  • Age less than 18 years old
  • Pregnant
  • Breast feeding
  • Allergy to Technetium-99m sulphur colloid
  • Presence of any of the conditions mentioned in the inclusion criteria

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - Minimum of 12 weeks to maximum of 18 months

Participants receive one of three first aid techniques (pressure bandage immobilisation, pressure pad, or no first aid) applied to the limb after injection with mock venom. The passage of mock venom is tracked by nuclear medicine imaging to evaluate first aid efficacy.

Repeated imaging visits for each first aid technique in a randomized order

Trial Site Locations

Total: 1 location

1

Queensland X-Ray

Hyde Park, Queensland, Australia, 4812

Actively Recruiting

Loading map...

Research Team

A

Adam L Holyoak

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

Similar Trials

Abnormalities of Plasma Willebrand Factor Activity Induced b...

Snake Envenomation

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial

Field trial of efficacy of local compression immobilization first-aid technique in Russell's viper (Daboia russelii siamensis) bite patients.

T Pe, S Mya, A A Myint...

https://pubmed.ncbi.nlm.nih.gov/11127337

Local compression pads as a first-aid measure for victims of bites by Russell's viper (Daboia russelii siamensis) in Myanmar.

Tun-Pe, Aye-Aye-Myint, Khin-Ei-Han...

https://pubmed.ncbi.nlm.nih.gov/7660439