ClinicalTrials.Veeva

Menu

Esthetic, Clinical and Radiographic Outcomes of Immediate and Delayed Implant Placement

Sun Yat-sen University logo

Sun Yat-sen University

Status

Enrolling

Conditions

Jaw, Edentulous, Partially
Acquired Absence of Single Tooth

Treatments

Procedure: Type 3 implant placement
Procedure: Type 1 implant placement

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this prospective cohort study is to compare the esthetic, clinical and patient-centered outcomes following immediate and delayed implant placement protocols.

Full description

Patients are divided into two groups: immediate and delayed implant placement. The investigators are asking subjects to take part in a research study of soft tissue and bone healing around dental implants following tooth extraction. The investigators want to compare how the gums and the bone changes shape with healing in two different scenarios.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • At least 18 years old and able to understand an informed consent
  • Adequate oral hygiene to allow for implant therapy consistent with standards of care.
  • Missing a single tooth in the maxillary anterior region
  • Presence of adjacent natural teeth

Exclusion criteria

  • Poor oral hygiene
  • Severe parafunctional habits, for example, bruxing and clenching
  • Presence of clinically active periodontal disease as expressed by probing pocket depths≥4 mm in combination with bleeding on probing.
  • Conditions that might lead to a possibly lowered regenerative capacity of the bone, for example, osteoporosis and Paget's disease
  • Pregnant or expecting to be pregnant
  • History of drug and alcohol abuse
  • History of systemic diseases that would contraindicate oral surgical treatment, for example, uncontrolled diabetes (defined as HBA1c level >7%)
  • Radiotherapy in the head and neck area,
  • On certain medications like bisphosphonates or steroids currently or within the past three months
  • Absence of adjacent teeth
  • Unwillingness to return for the follow-up examination
  • Smokers (more than 20 cigarettes per day). Subjects smoking <20 cigarettes per day were requested to stop smoking before and after surgery

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Type 1 implant placement
Active Comparator group
Description:
Implant is placed immediately following tooth extraction in one surgical procedure
Treatment:
Procedure: Type 1 implant placement
Type 3 implant placement
Active Comparator group
Description:
Implant is placed in the site which is left to heal for 3 months following tooth extraction
Treatment:
Procedure: Type 3 implant placement

Trial contacts and locations

1

Loading...

Central trial contact

Baoxin Huang; Xin Liu

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems