CClinicalTrials.gg
Not yet recruitingNCT07374757ILHAUpdated Jan 29, 2026

Immediately Loaded Implants With or Without Horizontal Augmentation

An interventional study of guided bone regeneration technique and No intervention in Bone Augmentation Associated With Immediate Loading, sponsored by Universidad Complutense de Madrid. Not yet recruiting. Open to participants aged Up to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-29.

Sponsored by Universidad Complutense de Madrid · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Non-randomized
Ages
Up to 18 Years
Sex
All
01

Study summary

This study aims to compare the clinical success and patient-reported outcomes of immediately loaded dental implants placed in sites with buccal dehiscence treated by horizontal augmentation versus immediately loaded implants placed without regeneration techniques.

Read the detailed description

This is a prospective, interventional, non-randomized, comparative clinical trial designed to evaluate the clinical outcomes of immediately loaded dental implants using two different surgical approaches. One group will receive implants placed in sites with buccal dehiscence treated by horizontal bone augmentation, while the comparison group will receive immediately loaded implants placed without the use of any bone regeneration techniques.

The primary outcome of the study is implant success at 12 months after implant placement. Secondary outcomes include marginal bone level changes, complication rates, and oral health-related quality of life assessed using a validated questionnaire. The study is conducted with a parallel assignment model and an open-label design due to the nature of the surgical interventions.

02

Conditions studied

  • Bone Augmentation Associated With Immediate Loading

Keywords

  • Inmediate loading
  • horizontal bone regeneration
03

In context

Lead sponsor

Universidad Complutense de Madrid is the lead sponsor of 200 studies on the registry; 60 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

Adult patients requiring dental implant placement Presence of buccal dehiscence at the implant site Indication for immediate loading Ability to provide written informed consent

Exclusion criteria

Exclusion Criteria:

Uncontrolled systemic diseases Active periodontal disease Heavy smoking exceeding predefined limits Conditions contraindicating oral surgery

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    Horizontal bone augmentation associate with immediate loading

    Horizontal bone augmentation associate with immediate loading

    Procedure: guided bone regeneration technique

  • Other
    Inmediate Loading without bone regeneration technique

    Immediately loaded dental implants placed without the use of any bone regeneration or augmentation techniques.

    Procedure: No intervention

Interventions

  • Procedureguided bone regeneration technique

    Immediately loaded dental implants placed in sites presenting buccal dehiscence treated by horizontal bone augmentation using a guided bone regeneration technique according to a standardized surgical protocol.

  • ProcedureNo intervention

    Immediately loaded dental implants placed without the use of any bone regeneration or augmentation techniques.

06

What researchers measure

Primary outcomes

  1. Implant Success Rate

    Implant success is defined as implant survival at 12 months, absence of clinical mobility, absence of persistent pain or infection, absence of peri-implant radiolucency, and no need for implant removal or surgical re-intervention.

    Time frame: 12 months after implant placement

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 29, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07374757
Lead sponsor
Universidad Complutense de Madrid
Responsible party
Sponsor
First posted
Jan 29, 2026
Start date
Jan 8, 2026 (estimated)
Primary completion
Dec 2026 (estimated)
Completion
Dec 11, 2027 (estimated)
Last update
Jan 29, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion