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