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Lacerations clinical trials

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NCT ID: NCT03957304 Completed - Laceration Repair Clinical Trials

Intranasal Dexmedetomidine Dose-finding Study

Start date: February 20, 2020
Phase: Phase 2
Study type: Interventional

The most common injury prompting an emergency department (ED) visit in children is a cut (laceration) that requires repair using stitches or skin glue. Despite anesthetic (freezing), laceration repair is often very distressful because in young children, most occur on the face. There is currently no effective drug to relieve the distress of laceration repair in children. The goal is to find a safe and effective drug to reduce distress in children undergoing laceration repair. Dexmedetomidine is a new drug that safely provides mild sedation and can be given as a painless nasal spray. Intranasal dexmedetomidine (IND) has been shown to reduce distress in children undergoing painful procedures such as dental work and intravenous insertion. However, no large study has explored IND for laceration repair. In order for research to change the way we care for children, a large study that enrolls children across many paediatric EDs needs to be performed. The first step is to conduct a smaller study to identify the safest and most effective dose. The proposed study plans to enroll 55 children age 1-10 years who require laceration repair.

NCT ID: NCT03880552 Completed - Delivery; Trauma Clinical Trials

Perineal Body Length and Perineal Lacerations

Start date: December 1, 2018
Phase:
Study type: Observational

The aim of this study was to evaluate the relationship between perineal body length and perineal laceration risk in primigravid patients. Primigravid women with singleton pregnancies in the first stage of labor at the 35th week of gestation were included in the study. The peineal body length of the patients was measured by the same physician.

NCT ID: NCT03830515 Recruiting - Wounds Clinical Trials

Evaluation of microMend Device to Close Lacerations

Start date: April 20, 2018
Phase: N/A
Study type: Interventional

In this study, total of 20 subjects will have lacerations will be closed with microMend, which is an FDA-listed wound closure product. microMend is a wound closure device that is the size and shape of a butterfly bandage and incorporates tiny Microstaples into an adhesive backing. Assessments by practitioners and Subjects of microMend will be made at Days 0 10, and 3 months using a combination of questionnaires and photographs.

NCT ID: NCT03688880 Terminated - Wounds and Injuries Clinical Trials

A Clinical Study to Compare MAR-CUTIS With Dermabond Advanced

Start date: October 30, 2018
Phase: N/A
Study type: Interventional

This was a randomized, open-label, multicenter, comparator-controlled clinical study to compare MAR-CUTIS with Dermabond Advanced in closure of surgical incisions and lacerations less than or equal to (<=)15 centimeter (cm). Eligible participants were randomized 2:1 to MAR-CUTIS or Dermabond Advanced.

NCT ID: NCT03685565 Completed - Facial Laceration Clinical Trials

Facial Lacerations Repaired With Dermabond Compared With Dermabond With Underlying Steristrips in Pediatric Patients

Start date: September 15, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is to compare cosmetic outcomes of simple facial lacerations in children repaired with Dermabond (skin glue) compared with Dermabond (skin glue) with underlying steristrips (skin adhesive strips).

NCT ID: NCT03681717 Recruiting - Laceration Clinical Trials

Virtual Reality vs. Standard-of-Care for Comfort During Laceration Repair

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

Lacerations are a common reason for presentation to the Emergency Department and children needing laceration repair with sutures are experiencing pain and anxiety. Virtual Reality (VR) is an immersive experience using sight, sound, and position sense. Using VR may enhance distraction during the painful procedure and may reduce attention to pain. This study will randomize children (6 - 16 years old) to receive Virtual Reality or standard of care in addition to pharmacoanalgesia during a laceration repair procedure. Investigators will measure pain, anxiety, satisfaction, amount of analgesia and the length of procedure and compare between the two groups.

NCT ID: NCT03641053 Completed - Wounds and Injuries Clinical Trials

Honey Versus Povidone-iodine on Laceration Wounds

Start date: January 29, 2018
Phase: Phase 3
Study type: Interventional

This study evaluates healing time in usage of honey and povidone-iodine over paraffin gauze as dressings in the treatment of acute laceration wounds. In Indonesia, especially in rural area, where most of the resources is limited and modern dressings are expensive and hard-to-find. The investigators tried to find an alternative which was easier to find and could act as a substitute of modern wound dressing. The hypothesis of this study is honey and povidone-iodine could be a good substitute (or equal to) to paraffin gauze on acute laceration wounds. Honey is chosen because of its versatility and already well-known to be used as a chronic wound dressing. Povidone-iodine was chosen as another alternative because it is still one of the most used substance in rural area as a wound dressing, but there is not enough study to support the usage of this substance. Paraffin gauze was chosen as a representative of modern wound dressing because it fulfilled the standard of wound dressing on acute wound, which is non-adherent and also moist.

NCT ID: NCT03628690 Recruiting - Laceration of Skin Clinical Trials

A Post-Market Study of BandGrip in Traumatic Wound Closure Compared to Suture

Start date: July 15, 2018
Phase: N/A
Study type: Interventional

an unbalanced (2:1) randomized study comparing two methods of traumatic skin closure in an ER setting: BandGrip vs suture

NCT ID: NCT03528512 Terminated - Laceration of Skin Clinical Trials

IN Ketamine vs IN Midazolam and Fentanyl for Laceration Repair

Start date: September 4, 2018
Phase: Phase 4
Study type: Interventional

Often, repair of the cuts (laceration repair) proves to be traumatic for the children and the parents. Nasal spray (Intranasal/IN) approaches for procedural pain reduction, such as during dental work, have been demonstrated to make drug administration painless and well tolerated. We are comparing IN ketamine to IN midazolam and fentanyl for pain and reducing anxiety during repair of cuts in children.

NCT ID: NCT03499002 Withdrawn - Laceration Clinical Trials

Teaching Medical Students How to Suture: Standard Simulation vs in Situ

Start date: April 2018
Phase: N/A
Study type: Interventional

The purpose of this project is to compare in situ simulation with standard lab simulation. To do this, 30 pre-clinical medical students will be randomized into the lab or ER and taught how to suture a simple laceration. To do this, a synthesized 'skin' will be placed over a volunteer's arm and will have an incision of a predetermined length.