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Идёт набор NCT06943053

Evaluation of Ioband Coverage Waterproof Dressing Versus Isolated Waterproof Dressing After Primary Total Knee Arthroplasty

Без фазы С лечением Postoperative Wound Care After TKA

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Isolate waterproof dressing (Opsite), Ioban coverage group.
Кому может быть актуально
Состояния в реестре: Postoperative Wound Care After TKA. Базовые параметры: от 55 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Таиланд
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Does Ioband Coverage Waterproof Dressing Provide Better Outcome Than Isolate Waterproof Dressing After Primary Total Knee Arthroplasty? A Prospective Randomized Controlled Trial

Обзор

Title: Evaluation of Ioband® Coverage Waterproof Dressing in Post-Operative Total Knee Arthroplasty (TKA) Goal: To evaluate the effectiveness of Ioband® coverage waterproof dressing compared to standard waterproof dressing in reducing dressing change frequency and peel-off degree post-op TKA. Main Research Questions: 1. Does Ioband® coverage waterproof dressing significantly decrease the degree of peel-off compared to standard waterproof dressing? 2. Does Ioband® coverage reduce the number of wound dressing changes required post-operatively? 3. Does Ioband® coverage improve overall patient satisfaction compared to standard waterproof dressing? Participants: Participants will include patients who have undergone total knee arthroplasty (TKA). Main Tasks and Interventions: 1. Randomization: Participants will be randomly assigned to receive either the Ioband® coverage waterproof dressing or the standard waterproof dressing. 2. Application of Dressings: Participants will have the assigned dressing applied to their surgical site post-operatively. 3. Assessment of Peel-Off Degree: Participants will undergo assessments to evaluate the degree of peel-off of the dressing over a specified time. 4. Wound Dressing Changes: Participants will have their dressing changed as per routine care protocols, with documentation of the number of changes. 5. Patient Satisfaction Survey: Participants will complete a satisfaction survey to assess their experiences with the dressing and overall comfort. Conclusion: The trial aims to provide insights into the benefits of Ioband® coverage waterproof dressing in improving post-operative care for TKA patients, focusing on key outcomes related to dressing performance and patient satisfaction.

Подробное описание

Study Design:

* Participants: 96 patients undergoing TKA, randomly assigned to two groups of 48 each: * Intervention Group: Ioband® coverage waterproof dressing * Control Group: Standard waterproof dressing (Opsite®)

Randomization Method:

-Computerized block randomization performed by an independent research assistant.

Pre-operative Procedures:

* Pre-emptive Analgesia administered 1 hour before surgery included:

1. Naproxen (250 mg) 2. Omeprazole (20 mg) 3. Acetaminophen (500 mg) 4. Pregabalin (75 mg)

Anesthesia: Administered spinal anesthesia and ultrasound-guided adductor canal block by experienced anesthesiologists.

Surgical Preparation: * Incision sites were prepped and draped using sterile technique. * Antiseptic Ioband® (60×45 cm) covered the incision site to prevent contamination.

Surgical Technique:

* Utilization of a standard medial parapatellar approach with a minimally invasive TKA technique. * A tourniquet was inflated to 100 mmHg above systolic blood pressure and was deflated after wound closure. * Cemented posterior stabilizer prosthetics (Nexgen LPS) and patellar resurfacing were used. * Anesthetic cocktail (0.5% bupivacaine, adrenaline, ketorolac, morphine) was injected around the capsule after prosthesis insertion.

Post-operative Care:

* No suction drains or extremity wraps used. * Wounds closed with waterproof dressing (Opsite® size 25×10 cm) in 90-degree knee flexion without tension. * Pain Management: Multimodal pain control was employed. * Antibiotic Prophylaxis: Administered for 24 hours post-surgery. * Rehabilitation: Early knee range of motion exercises and ambulation were encouraged within 24 hours post-operation.

Wound Management Protocol:

* Patients were allowed to start bathing 48 hours post-op. * Dressing change on post-op day 3, using sterile technique: * Control Group: Covered with waterproof dressing (Opsite®). * Intervention Group: Covered with Ioband® in knee flexion.

Wound Care Instructions:

* Keep covering material dry and clean; avoid irritation. * Report any signs of infection (redness, swelling, fever) to a doctor. * Avoid creams or powders unless prescribed. * Avoid scratching or rubbing around the wound. * Light activities permitted; avoid strenuous activities for 6 weeks. * Dressing should not be changed until advised, typically after 14 days unless signs of complications are observed.

Criteria for Dressing Change:

* Change dressing if: * First waterproof dressing peels off grade II or III. * Second dressing has over 50% bleeding. * Suspected surgical site infection. Patients were also included in a chat group for wound care consultation.

Вмешательства

  • Устройство Isolate waterproof dressing (Opsite)
    Application of standard Opsite® waterproof dressing directly over the surgical incision following primary total knee arthroplasty. No additional drape or coverage was applied. The dressing remained in place until removal.
  • Устройство Ioban coverage group
    Application of Ioban® iodine-impregnated antimicrobial incise drape over the standard waterproof dressing following primary total knee arthroplasty. The Ioban drape extends 2 cm beyond all edges of the dressing and remains in place until removal.

Первичные конечные точки

  • Number of change wound dressing [Срок оценки: 14 days postoperation]
Вторичные конечные точки (4)
  • Degree of peel off wound [Срок оценки: 14 days postoperation]
  • Satisfactory of patient [Срок оценки: 14 days post-operation]
  • Post op Range of motion of knee [Срок оценки: At 2 weeks, 6 weeks and 3 months postoperation]
  • Wound-related Complication [Срок оценки: At 2 weeks, 6 weeks and 3 months postoperation]

Критерии участия

Критерии включения

  • Primary unilateral TKA
  • Age 55-80 yrs

Критерии исключения

  • Chronic Skin disease such as Psoriasis
  • Chronic steroid use
  • Allergy to skin adhesive, Cover wound
  • Robotic TKA
  • Iodine allergy
  • Not follow protocol

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Таиланд · 2 центра
  • Thammasat University Hospital — Pathum Thani
  • Department of Orthopaedics, Thammasat University — Pathum Thani

Публикации

  • 1 Primary Total Knee Replacement: A Recipe for Dry Dressing Azfar KM, Adil AO, Tarig AR, Adel G. Primary Total Knee Replacement: A Recipe for Dry Dressing. Cureus. 2023;15(4). 2 The effect of different wound dressing materials used in postoperative treatment of wounds after total hip arthroplasty and total knee arthroplasty: A meta-analysis Yingjia Yuan, Jin Li, Ke Wang, Guanqiang Zheng, Shengting

Идентификаторы

NCT: NCT06943053 · TUH wound coverage after TKA

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗