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Comparison of Er:YAG Assisted Laser Crown Lengthening Against Surgical Crown Lengthening

16 de junio de 2026 actualizado por: Gulf Medical University

Comparison of Er:YAG Assisted Laser Crown Lengthening Against Surgical Crown Lengthening: a Longitudinal Study.

Crown lengthening is a clinical procedure that involves reshaping the gingiva, and sometimes bone, in order to expose more of tooth's structure. The procedures is performed for both functional and aesthetic reasons. In certain instances, this procedure is performed to This procedure is commonly performed for both functional and aesthetic reasons, such as to prepare a tooth for a crown or to enhance the appearance of a smile. Traditional crown lengthening techniques typically involve surgical methods that can be invasive, leading to extended recovery times and postoperative discomfort in this study we compare traditional versus the laser aided crown lengthening to compare the periodontal parameters in both cases.

Descripción general del estudio

Descripción detallada

Crown lengthening is a clinical procedure that involves reshaping the gingiva, and sometimes bone, in order to expose more of tooth's structure. The procedures is performed for both functional and aesthetic reasons. In certain instances, this procedure is performed to This procedure is commonly performed for both functional and aesthetic reasons, such as to prepare a tooth for a crown or to enhance the appearance of a smile. Traditional crown lengthening techniques typically involve surgical methods that can be invasive, leading to extended recovery times and postoperative discomfort in this study we compare traditional versus the laser aided crown lengthening to compare the periodontal parameters in both cases.

Laser technology and minimally invasive therapy have become increasingly prominent in various dental fields. The erbium:YAG laser, the newest type, can be used on both soft and hard tissues. This study evaluates the periodontal outcomes of a flapless crown lengthening procedure using the erbium:YAG laser in comparison to traditional methods.

Crown lengthening aims to obtain a larger crown surface by surgical means either by gingivectomy or by recontouring of the cortical bone. The obtained increased crown surface can be used to build crowns.

Conventional surgical techniques involve incisions, elevation of flap and osteoplasty. Subsequently, the flaps are approximated and sutured.

LASER stands for Light amplification by stimulated emission of radiation. Several lasers are used in dentistry including soft and hard tissue lasers. Soft tissue lasers including diode lasers are used to incise the soft tissue, whereas lasers including Er:YAG lasers hard tissue lasers can be used to Er:YAG lasers are known to have good cutting and coagulation abilities on soft tissues.(1) Upon use in soft tissues the laser provides good coagulation resulting in bleeding control. The laser is capable of Lasers offer significant advantages including reduced bacteraemia, reduced post operative discomfort, improved bleeding control and quicker healing. The comfort of avoiding a surgical procedure is an added advantage which may make the patient less concerned about opting for treatment options.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

26

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Nesma Shemais
  • Número de teléfono: 0529961988
  • Correo electrónico: dr.nesma@gmu.ac.ae

Ubicaciones de estudio

    • Ajman Emirate
      • Ajman, Ajman Emirate, Emiratos Árabes Unidos, 00000
        • Reclutamiento
        • Gulf Medical University
        • Contacto:
          • Nesma Shemais, PhD
          • Número de teléfono: 0529961988
          • Correo electrónico: dr.nesma@gmu.ac.ae

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Sí

Descripción

  • Inclusion criteria:

    1. Teeth indicated for crown lengthening procedure either in the maxillary or mandibular arch.
    2. Patients in the age group of 18-75 years.
  • Exclusion criteria:

    1. Patients with uncontrolled diabetes mellitus. Uncontrolled diabetes mellitus diagnosed with HbA1C ≥ 7% will be an exclusion criterion.
    2. Smokers (considered as smoking ≥ 10 cigarettes/day)
    3. Pregnant women
    4. Patients with uncontrolled systemic diseases that may affect the healing of soft and hard tissues of the periodontium will be excluded.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: crown lengthening using Er:YAG Laser
Er:YAG laser is used for both soft and hard tissue recontouring according to the manufacturer's guidelines. In the case of gingivectomy and soft tissue recontouring, 4x17mm, 0.6x17mm, and 1.3x17mm tips are used, and the soft tissue mode is selected on the device screen, which sets the device parameters to 100mJ x 20Hz. The tip is in direct contact with the soft tissue until the desired soft tissue level is achieved. For bone contouring, the hard tissue option is selected on the device's screen, setting the parameters to 150mJ x 20Hz. A non-contact approach is used to reshape the underlying bone.
Er:YAG laser is used for both soft and hard tissue recontouring according to the manufacturer's guidelines. In the case of gingivectomy and soft tissue recontouring, 4x17mm, 0.6x17mm, and 1.3x17mm tips are used, and the soft tissue mode is selected on the device screen, which sets the device parameters to 100mJ x 20Hz. The tip is in direct contact with the soft tissue until the desired soft tissue level is achieved. For bone contouring, the hard tissue option is selected on the device's screen, setting the parameters to 150mJ x 20Hz. A non-contact approach is used to reshape the underlying bone.
Comparador activo: : conventional surgical crown lengthening by opening envelop flap

Bevel incision with number 15 blades is place on the margin following with sulcular incision and excess gingival tissues are removed using Gracey currets .in case if any granulation tissues are seen it should be removed and washed with saline.

Following with bone recontouring and reshaping after periosteal elevator is used to expose the underlying bone. fissure burs or coarse diamond stones are used until thing bone tissues are left over the root and rest can be removed with scaler to prevent damage to the tooth.

Resorbable sutures are place after the surgery and the case is followed up for 3 months period.

In the case of conventional surgical crown lengthening, after delivering the local anesthetic solution to the surgical area, soft tissue recontouring starts. This procedure, which involves excising the soft tissue with a gingivectomy, is typically done to improve aesthetics or create more space for better restoration seating. The gingival border is typically 1 mm coronal to the CEJ

Bevel incision with number 15 blades is place on the margin following with sulcular incision and excess gingival tissues are removed using Gracey currets .in case if any granulation tissues are seen it should be removed and washed with saline.

Following with bone recontouring and reshaping after periosteal elevator is used to expose the underlying bone. fissure burs or coarse diamond stones are used until thing bone tissues are left over the root and rest can be removed with scaler to prevent damage to the tooth.

Resorbable sutures are place after the surgery and the case is followed up for 3 months period.

In the case of conventional surgical crown lengthening, after delivering the local anesthetic solution to the surgical area, soft tissue recontouring starts. This procedure, which involves excising the soft tissue with a gingivectomy, is typically done to improve aesthetics or create more space for better restoration seating. The gingival border is typically 1 mm coronal to the CEJ.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Postoperative Pain
Periodo de tiempo: baseline, 3 days
VAS 0-10
baseline, 3 days
Postoperative pain
Periodo de tiempo: baseline 3 days
VAS scale 0-10
baseline 3 days

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Probing depth
Periodo de tiempo: baseline, 3 months , 6 months
baseline, 3 months , 6 months
patient satisfaction VAS
Periodo de tiempo: baseline, 3 days , 6 months
VAS 0-10
baseline, 3 days , 6 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de julio de 2025

Finalización primaria (Estimado)

1 de septiembre de 2026

Finalización del estudio (Estimado)

30 de septiembre de 2026

Fechas de registro del estudio

Enviado por primera vez

10 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

16 de junio de 2026

Publicado por primera vez (Actual)

17 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

17 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

16 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Palabras clave

Otros números de identificación del estudio

  • Ali-MDSperio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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