Immediate vs conventional implants after atraumatic extraction in upper premolars

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study compares two implant strategies following atraumatic extraction: immediate placement and loading of compressive implants versus conventional delayed placement. It aims to measure effectiveness, bone loss, and implant survival between the two approaches. Eligible participants are adults aged 20–40 who need implants for badly damaged upper premolars, are non-smokers, and free of systemic conditions affecting healing. The study protocol involves surgical placement of implants and immediate functional loading with suitable prosthetics, with follow-up to assess outcomes. The evidence will inform whether rapid restoration provides advantages without compromising health or longevity of implants.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Medically free patient
* Males and females
* Non-smoker patients
* Age ranging from 20-40 years
* Badly destructed upper premolar teeth that require implants, bone covering 2/3 of the root and of sufficient bone volume.

Exclusion Criteria:

* Patients with systemic conditions known to affect the periodontal status and healing such as uncontrolled diabetes and osteoporosis
* Heavy smokers
* Unfavorable position of the tooth or remaining roots
* Vitamin D deficiency,
* Periapical lesion/ periodontal affection

Where it's running

• Beni-suef university
  Banī Suwayf, Egypt Recruiting

Study contacts

• Study coordinator: ahmed alghandour, phd
• Email: ahmed.nagi@dent.bsu.eg
• Phone: 01224567435

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Concomitant TURP with bladder stone surgery vs bladder stone surgery alone in men with BPH

  This study tests whether adding TURP at the time of bladder stone surgery helps men with BPH have better short-term outcomes.

  Recruiting Beni-Suef University · Banī Suwayf, Beni Suweif Governorate · NCT07831486

• Emergency urinary drainage followed by PCNL in obstructive urosepsis

  Doctors test whether the method of emergency drainage (retrograde ureteral stent or percutaneous nephrostomy) affects how well patients do after undergoing definitive PCNL.

  Recruiting Beni-Suef University · Banī Suwayf, Beni Suweif Governorate · NCT07826325

• Palmitoylethanolamide for Central Sensitisation and Neuroinflammation in Chronic Low Back Pain

  A treatment with palmitoylethanolamide is being tried to see if it helps people with chronic low back pain who have nerve-related pain and disc problems.

  Recruiting Beni-Suef University · Banī Suwayf · NCT07772141

• Nebulized dexmedetomidine for early chronic migraine

  This study tests whether inhaled dexmedetomidine can lessen central sensitization and help prevent chronification in people with early chronic migraine.

  Recruiting Beni-Suef University · Banī Suwayf · NCT07769255

• Integrated neuromuscular inhibition, dry cupping, and dry needling for neck pain

  This trial tests four treatment setups to see which helps people with chronic neck muscle pain best, all alongside standard physical therapy.

  Recruiting Beni-Suef University · Giza · NCT07711041

• See if empagliflozin helps kidney function in people with lupus nephritis

  This study tests whether adding empagliflozin to standard care improves kidney function in adults with active lupus nephritis.

  Recruiting Phase 4 Beni-Suef University · Banī Suwayf · NCT07700940

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.