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amnion allograft for increasing the width of peri-implant attached mucosa

Comparison of amnion allograft with free gingival graft to improve the attached mucosa around dental implants

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016101621069N2
Enrollment
28
Registered
2017-03-16
Start date
2017-04-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

lack of attached mucosa around dental implants. Gingival recession

Interventions

Intervention 1: In the control group, participants recieve free gingival graft (from palate) to increase the width of attached mucosa around implants. In the test group, patients are treated with amni
Treatment - Surgery
In the control group, participants recieve free gingival graft (from palate) to increase the width of attached mucosa around implants. In the test group, patients are treated with amniotic allogenic m
in test group, the attached peri-implant mucosa is augmented using allogenic amniotic membrane. in the control group, free gingival graft from the palatal mucosa is performed to increase the attached

Sponsors

Iranian Tissue Bank Research Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: inclusion criteria: patients age more than 18 years; systemic and periodontal health; at least one implant with less than 1 mm attached mucosa after the stage 1 implant insertion surgery; favorable plaque control (less than 20% olery plaque index); patients should be able to afford the related procedures.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Width of attached peri-implant mucosa. Timepoint: before surgery, immediately after surgery, after the 1st, 2nd, 6th and 12th postoperative weeks. Method of measurement: measurement of the distance between mucosal margin to the mucogingival line in the midbuccal of each implants using UNC-15 periodontal probe - probing depth.

Secondary

MeasureTime frame
Post-operative pain. Timepoint: after the 1st, the 2nd, the 6th and the 12th postoperative weeks. Method of measurement: visual analogue scale (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Babazade

school of dentistry, TUMS

hossein.babazade89@gmail.com+98 21 8835 1170

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026