[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100636711":3},{"organization":4,"armGroups":7,"interventions":17,"overallOfficials":23,"centralContacts":23,"locations":23,"responsibleParty":36,"collaborators":40,"id":43,"slug":44,"hasResults":45,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":23,"eligibilityCriteria":49,"healthyVolunteers":50,"sex":51,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":23,"studyType":57,"phases":58,"briefSummary":60,"conditions":61,"keywords":66,"overallStatus":75,"whyStopped":23,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":23},{"fullName":5,"class":6},"University of Jordan","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Suture Comparison Group","EXPERIMENTAL","A single group of 60 participants. Each participant serves as their own control (split-mouth design). Every participant will receive four different suture materials placed in four distinct sites (Anterior Buccal, Posterior Buccal, Anterior Palatal, Posterior Palatal) in the maxillary arch.",[13,14,15,16],"Device: Silk Suture (Braided, Non-absorbable)","Device: Polyglactin 910 Suture (Braided, Absorbable)","Device: Polyamide Suture (Monofilament, Non-absorbable)","Device: Poliglecaprone 25 Suture (Monofilament, Absorbable)",[18,24,28,32],{"type":19,"name":20,"description":21,"armGroupLabels":22,"otherNames":23},"DEVICE","Silk Suture (Braided, Non-absorbable)","4-0 Black Braided Silk suture. Used for soft tissue approximation.",[9],null,{"type":19,"name":25,"description":26,"armGroupLabels":27,"otherNames":23},"Polyglactin 910 Suture (Braided, Absorbable)","4-0 Synthetic braided absorbable suture (e.g., Vicryl).",[9],{"type":19,"name":29,"description":30,"armGroupLabels":31,"otherNames":23},"Polyamide Suture (Monofilament, Non-absorbable)","4-0 Nylon monofilament suture.",[9],{"type":19,"name":33,"description":34,"armGroupLabels":35,"otherNames":23},"Poliglecaprone 25 Suture (Monofilament, Absorbable)","4-0 Synthetic monofilament absorbable suture (e.g., Monocryl).",[9],{"type":37,"investigatorFullName":38,"investigatorTitle":39,"investigatorAffiliation":5,"oldNameTitle":23,"oldOrganization":23},"PRINCIPAL_INVESTIGATOR","Omar Amjad Karadsheh","Associate Professor, Department of Periodontology",[41],{"name":42,"class":6},"Jordan University Hospital","100636711","patient-reported-outcomes-of-four-intraoral-suture-materials-100636711",false,"NCT07569237","Patient-Reported Outcomes of Four Intraoral Suture Materials","Patient-Reported Outcomes Following Application of Intraoral Sutures: A Split-Mouth Randomized Controlled Trial","Inclusion Criteria:\n\nAdults aged 20-30 years.\n\nSystemically healthy (ASA I-II).\n\nNo history of allergy to study suture materials.\n\nPeriodontally healthy, with no active oral lesions, including carious lesions.\n\nDental Requirements: All maxillary canine, second premolar, and first molar teeth present.\n\nMinimal (≤0.5 mm) open contacts between the pairs of teeth that define the study sites.\n\nIdeally, full maxillary dentition present from first molar to first molar.\n\nAt least 2 mm of keratinized tissue width on buccal intervention sites.\n\nWilling and able to provide informed consent.\n\nWilling and able to attend all study follow-up visits and complete study questionnaires.\n\nExclusion Criteria:\n\nAllergy to any study materials (e.g., suture materials or anesthetics) or medications (Paracetamol).\n\nAny systemic disease affecting wound healing (e.g., diabetes, immunosuppression).\n\nUse of any medications.\n\nPregnancy or lactation.\n\nUnwillingness or inability to provide informed consent.\n\nUnwillingness or inability to comply with study protocol and follow-up visits.\n\nExit Criteria:\n\nParticipants may exit the study at any time if they wish to discontinue participation.\n\nNoncompliance with study protocol and visits.\n\nDevelopment of conditions (e.g., infection) that require immediate care or that introduce exclusion criteria.",true,"ALL","20 Years","30 Years",{"count":55,"type":56},60,"ESTIMATED","INTERVENTIONAL",[59],"NA","When patients undergo minor oral surgery, dentists use various types of stitches (sutures) to help the gums heal. These stitches can be made of different materials, and some might feel more comfortable, cause less pain, or interfere less with eating and speaking than others.\n\nThe purpose of this study is to compare four commonly used dental suture materials to see which ones patients prefer. Participants in this study will receive four different types of stitches in different areas of their upper jaw after a routine dental procedure.\n\nPatients will be asked to report their levels of pain, discomfort, and any difficulties with daily activities like eating and talking on Days 3, 7, and 14 after the procedure. A panel of dental specialists will also examine photos of the healing process to see if one material helps the mouth heal better than others. This research will help dentists choose the best materials to improve patient comfort after oral surgery.",[62,63,64,65],"Suture Materials","Wound Healing","Patient Comfort","Oral Health-Related Quality of Life",[67,68,69,70,71,72,73,74],"Split-mouth design","Patient-reported outcome measures (PROMs)","Intraoral sutures","Dental surgery","Visual Analog Scale (VAS)","Periodontology","Oral surgery healing","Braided vs Monofilament sutures","NOT_YET_RECRUITING","2026-04-28",{"date":78,"type":79},"2026-05-06","ACTUAL",{"date":81,"type":56},"2026-07",{"date":83,"type":56},"2028-04",{"name":5,"class":6}]