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Search / Trial NCT01952964

The Effects of Anti-microbial Spray Dressing in Preventing Tenckhoff Catheter Exit Site Infection for End Stage Renal Failure Patients

Launched by THE QUEEN ELIZABETH HOSPITAL · Sep 25, 2013

Trial Information

Current as of June 18, 2025

Unknown status

Keywords

Exit Site Infection Skin Allergy Physical Damage

ClinConnect Summary

Methods

The study will be conducted using randomized controlled trial.

Sampling

The subjects will be the patients with Tenckhoff Catheter recruited from the renal team in a regional acute hospital and a satellite dialysis centre. The sampling method will be convenience sampling. The subjects will be recruited sequentially after the insertion of Tenckhoff Catheter.

Inclusion criteria

* Patient with established Tenckhoff Catheter for at least 3 months
* Patient with skin condition healed satisfactorily

Exclusion criteria

* Patient presents with signs and symptoms of exit site infection...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • - Patient with established Tenckhoff Catheter for at least 3 months with skin healed satisfactorily
  • Exclusion Criteria:
  • Patient presents with signs and symptoms of exit site infection e.g. purulent discharge, pain, and swab of exit cultured with positive growth.
  • Patient with unhealed exit site.
  • Patient currently requires antibiotics
  • Patient shows sensitive to JUC Spray Dressing or 0.05% Chlorhexidine solution

About The Queen Elizabeth Hospital

The Queen Elizabeth Hospital, a leading healthcare institution, is dedicated to advancing medical research and improving patient outcomes through innovative clinical trials. With a strong emphasis on patient safety and ethical standards, the hospital collaborates with multidisciplinary teams to explore cutting-edge therapies and treatments across various medical fields. Committed to fostering scientific excellence, the Queen Elizabeth Hospital aims to translate research findings into practical applications that enhance healthcare delivery and contribute to the global medical community.

Locations

Hong Kong, , Hong Kong

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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