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Completed medical history will take for all patients. All patients' guardians were informed about the procedure, the possible postoperative complications, and requested to sign an informed consent that was translated into Arabic language.
Patients were randomly divided into two equal groups by means of sealed envelopes:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| metformin group | Experimental |
| |
| placebo group | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| metformin group | Procedure | - Group A: 18 patients who received a combination of illiac cancellous bone graft and 2ml of 1% metformin gel (20mg of metformin with 2% hydroxymethyl cellulose) |
| Measure | Description | Time Frame |
|---|---|---|
| bone density | by cone beam ct | 6 months postoperative |
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Inclusion criteria:
Exclusion Criteria:
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| placebo group | Procedure | - Group B: 18 patients who received illiac cancellous bone graft and 2 ml placebo gel (2% hydroxymethyl cellulose |
|