Alveolar Ridge Preservation Using Acemannan Aloe Vera Versus Natural Socket Healing
Radiographic And Histomorphometric Assessment Following Alveolar Ridge Preservation Using Acemannan Aloe Vera Powder Extract Versus Normal Socket Healing. A Randomized Clinical Trial
1 other identifier
interventional
26
1 country
1
Brief Summary
The goal of this clinical trial is to evaluate the effectiveness of acemannan aloe vera powder extract in preserving the alveolar ridge following tooth extraction in healthy adult patients. It will also assess the healing process by radiographic and histomorphometric analyses. The main questions it aims to answer are: Does acemannan aloe vera powder extract improve alveolar ridge preservation compared with natural socket healing? Does the use of acemannan aloe vera powder extract enhance bone quality and new bone formation as assessed by radiographic and histomorphometric outcomes? Researchers will compare sockets treated with acemannan aloe vera powder extract to sockets allowed to heal naturally to determine whether the intervention results in improved dimensional preservation of the alveolar ridge and enhanced bone regeneration. Participants will: Undergo tooth extraction according to the study protocol. Be randomly assigned to receive either acemannan aloe vera powder extract for alveolar ridge preservation or natural socket healing without grafting. Attend scheduled follow-up visits for clinical and radiographic evaluations. Undergo radiographic assessment using cone-beam computed tomography (CBCT) to evaluate changes in alveolar ridge dimensions. Provide a bone biopsy at the time of implant placement for histomorphometric analysis of new bone formation and tissue composition.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 12, 2025
CompletedFirst Submitted
Initial submission to the registry
July 20, 2026
CompletedFirst Posted
Study publicly available on registry
July 30, 2026
CompletedJuly 30, 2026
July 1, 2026
9 months
July 20, 2026
July 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in radiographic horizontal ridge width at 4 mm below the most coronal aspect of the crest
The immediate postoperative scans served as the baseline and were evaluated after 6 months to assess horizontal ridge width. Employing the same software, standardized measurements were obtained at both time points using consistent anatomical landmarks. On each baseline and after 6 months images, the apical point of the extraction socket was identified, and a vertical line was drawn through the socket's midpoint. A horizontal reference line perpendicular to the vertical axis was then established at the apical point. Horizontal ridge width was measured at 4 mm below the crest, yielding the parameters HW-4
6 months postoperatively
Secondary Outcomes (3)
Horizontal ridge width was measured at 2 mm and 6 mm below the crest
6 months postoperatively
Vertical ridge height
6-months post
Percentage of new vital bone formation
6 months post
Study Arms (2)
Socket Preservation with Acemannan Aloe Vera Extract Powder
EXPERIMENTALAfter atraumatic tooth extraction and socket debridement, the Aloe vera mixture was then prepared by combining a 500 mg of Aloe vera powder , equivalent to approximately ¼ teaspoon, with 2 ml of sterile saline (Nimma et al., 2017). The mixture was immediately applied into the extraction socket and gently condensed using a bone graft condenser. A collagen plug was carefully placed above the Aloe vera mixture in the socket, ensuring close contact with all socket walls. Finally, the site was closed and stabilized using Vicryl 5-0 resorbable sutures to secure the collagen plug and support proper healing during the early postoperative phase
Control Group (Normal Socket Healing)
ACTIVE COMPARATORFollowing extraction, the sockets were carefully debrided to remove any debris and blood clots. The sockets were then left to heal naturally without the application of any adjunctive biomaterials.
Interventions
After atraumatic tooth extraction and socket debridement, the Aloe vera mixture was then prepared by combining a 500 mg of Aloe vera powder , equivalent to approximately ¼ teaspoon, with 2 ml of sterile saline (Nimma et al., 2017). The mixture was immediately applied into the extraction socket and gently condensed using a bone graft condenser. A collagen plug was carefully placed above the Aloe vera mixture in the socket, ensuring close contact with all socket walls. Finally, the site was closed and stabilized using Vicryl 5-0 resorbable sutures to secure the collagen plug and support proper healing during the early postoperative phase .
Control Group: Normal Socket Healing * Tooth Extraction: Standard tooth extraction procedures will be followed, ensuring minimal trauma to the surrounding bone and soft tissues. * Socket Cleaning: The extraction socket will be thoroughly cleaned and debrided to remove any debris and blood clots. * Natural Healing: The socket will be allowed to heal naturally without any additional intervention. Standard post-extraction care will be provided.
Eligibility Criteria
You may qualify if:
- Non-restorable tooth in maxillary or mandibular anterior esthetic region.
- Intact or minimally affected buccal plate of bone.
- Patients at least 18 years or older.
- Motivated patients, agree to sign the written informed consent and complete the follow-up period.
You may not qualify if:
- Infection at the extraction site.
- Smokers more than 10 cigarettes per day .
- Patients undergoing or having a history of radiotherapy, chemotherapy, or bisphosphonate therapy .
- Systemic conditions that may compromise healing or bone metabolism (e.g., uncontrolled diabetes, hyperthyroidism) .
- Patients on medication that may interfere with healing (Corticosteroids, Bisphosphonate, Chemo/radio therapy)
- Systemic diseases or medications that affect blood clotting
- Pregnant females or those planning to get pregnant during the study period (American Dental Association, 2011).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Egypt Faculty of Dentistry Cairo University
Cairo, Egypt, 12613, Egypt
MeSH Terms
Interventions
Study Officials
- PRINCIPAL INVESTIGATOR
Nouf Saeed Alamoudi, Bachelor
Cairo University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator Nouf Alamoudi Master Degree student, Dental Imlantology department, Faculty of Dentistry, Cairo University
Study Record Dates
First Submitted
July 20, 2026
First Posted
July 30, 2026
Study Start
October 1, 2024
Primary Completion
July 1, 2025
Study Completion
December 12, 2025
Last Updated
July 30, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share