The Effect of Episiotomy Wound Care and Genital Hygiene Training on Episiotomy Wound Healing and Pain Perception: Randomized Controlled Trial
The World Health Organization (WHO) and professional societies recommend restricted episiotomy instead of routine episiotomy. However, since the 1990s, there has been evidence of the risks of the procedure, and although routine use has no benefit, it is still widely used. In this study, investigators aimed to determine the effect of episiotomy on the wound healing process and pain perception by providing episiotomy wound healing and genital hygiene training with training material created to raise awareness about wound care after episiotomy and to eliminate factors that delay the healing of episiotomy wound.
NCT05358236 — Pain
Status: Completed
http://inclinicaltrials.com/pain/NCT05358236/
Non-pharmacological Pain Care Using Virtual Reality Therapy or Music Therapy During Complex Wound Care in Adults at Surgical Nursing Wards
The main objective of this study is to evaluate the effect on pain and both Virtual Reality and Music Therapy as add-on therapy during wound care at the surgical wards in adults.
NCT05744024 — Virtual Reality
Status: Enrolling by invitation
http://inclinicaltrials.com/virtual-reality/NCT05744024/
Survey of Patients Who Have Been Prescribed a Topical Compound for Pain Management, Wound Care or Scar Care or to Patients Who Have Been Requested to do a Urinary Drug Test (UDT) by Their Provider.
This is a survey study that will be given to patients who have been prescribed a topical compound for pain management, wound care or scar care or to patients who have been requested to do a urinary drug test (UDT) by their provider. The initial survey for pain management, wound care, scar care or UDT will be given to the patient by their providers during their office visit.
NCT02195063 — Pain
Status: Recruiting
http://inclinicaltrials.com/pain/NCT02195063/
Integrated Client Care Project Randomized Control Trial: Wound Care Evaluation
This study will use a randomized control trial design to compare wound care clients who receive "integrated care" versus "usual care" in Community Care Access Centres (CCAC) in Ontario. Data will be collected by existing administrative databases and linked by the Institute for Clinical Evaluative Sciences (ICES). The researchers will analyze these databases and report findings.
NCT01573832 — Wound
Status: Completed
http://inclinicaltrials.com/wound/NCT01573832/
A Controlled Study Comparing Basic Wound Care to the Provant® Therapy System as an Adjunct to Basic Wound Care for Wound Surface Area Reduction in Diabetic Plantar Foot Wounds
The objective of this study is to compare the reduction in wound surface areas between patients with diabetic ulcers utilizing Provant's pulsed radio frequency energy therapy (PRFE) as an adjunct to standardized basic wound care to those utilizing standardized basic wound care alone.
NCT00761176 — Diabetic Foot Ulcers
Status: Terminated
http://inclinicaltrials.com/diabetic-foot-ulcers/NCT00761176/
Prospective Randomized Trial of Standard Wound Care Versus Standard Wound Care Plus Shock Wave Therapy for Traumatic Wounds of the Extremity
The purpose of this study is to determine if adding shock wave therapy to standard-of-care wound treatment for traumatic extremity wounds helps them heal faster.
NCT00486733 — Soft Tissue Injuries
Status: Recruiting
http://inclinicaltrials.com/soft-tissue-injuries/NCT00486733/
The Effect of Pressure Wound Care Package on O.R. Pressure Wound Development
SUMMARY In a non-randomised (quasi-experimental) clinical study, it was aimed to determine the effect of the care package applied in the early postoperative period on operating theatre pressure sores, pain, fear of falling and comfort in patients undergoing orthopaedic surgery. In the study, the care bundle for pressure injuries was prepared in accordance with the clinical guidelines and was applied to the patients in the study group. This study was conducted in the orthopaedics and traumatology clinic of a public hospital in the Southeastern Anatolia Region of Turkey.
NCT05852236 — Pressure Injury
Status: Completed
http://inclinicaltrials.com/pressure-injury/NCT05852236/
Investigation of the Effects of Topical Haemoglobin Wound Care Spray in Pressure Ulcer Care
A prospective randomised controlled experimental study was planned to compare the effects of pressure sore dressing using topical haemoglobin and traditional gauze dressing using saline on the healing process and cost of pressure sores in patients with pressure sores.
NCT05915169 — Pressure Ulcer
Status: Recruiting
http://inclinicaltrials.com/pressure-ulcer/NCT05915169/
Clinical Evaluation of the SNaP Wound Care System in Promoting Healing in Chronic Wounds
The purpose of this study is to evaluate a novel topical negative pressure (TNP) wound therapy device called the SNaP® (Smart Negative Pressure) Wound Care System for the treatment of lower extremity diabetic, venous and mixed aetiology leg wounds.
NCT01417208 — Lower Extremity Mixed Aetiology Leg Wounds
Status: Withdrawn
http://inclinicaltrials.com/lower-extremity-mixed-aetiology-leg-wounds/NCT01417208/
Obtaining and Storing Standard of Care Wound Biopsies for Immediate or Future Wound Related Scientific Study
The objective of this study protocol is to use wound biopsies that have been obtained during standard of care management for further scientific evaluation after standard evaluation by a pathologist. Further imaging and molecular analyses would closely evaluate the presence, architecture, and interaction of wound biofilm and human host tissues.
NCT00759889 — Diabetic Foot
Status: Completed
http://inclinicaltrials.com/diabetic-foot/NCT00759889/