Purpose: To compare the safety and e cacy of subconjunctival injection of Mitomycin C(MMC) with sponge-applied MMC during trabeculectomy.Methods: This prospective, randomized, interventional study was conducted on consecutive patients with uncontrolled glaucoma. 137 patients were randomized into an Injection group(Group 1,n=66) and a sponge group(Group 2,n=71).Trabeculectomy was performed in all patients who were followed up on days 1, 15, 30, 3 months,6 months,1 year,2 years & 3 years postoperatively. Baseline & follow-up visits were compared to nd out difference in the number of antiglaucoma medications (AGM ), Intraocular pressure(IOP), and Best Corrected Visual Acuity(BCVA).In Group 1, the surgeon used MMC 0.2 mg/ml as subconjunctival injection and two separate semicircular surgical sponges soaked with MMC solution of 0.2 mg/mL were inserted subconjunctivally in Group 2.Results:Mean preop IOP was 34.21±13.3mmHg& 34.17±10.6mmHg in group 1&2 respectively,which reduced to 11.34±3.7& 12.57±4.7mmHg(6 months),11.97±4.2& 13.60 ±5.3mmHg(1year),12.42±4.4& 11.77±2.8 mmHg(2years)&11.25±3.2&11.81±3.2mmHg at nal visit(P<0.001 in both groups)with no signi cant difference between the groups.The mean number of preoperative AGM was 2.32±0.7&2.32±0.8 in group1&2 respectively which reduced to 0.78±0.9(P<0.001)&1.13±1.1(P=0.930)at 3 years.Overall success rates were 75.3% in group 1 and 70.7% in group 2 at 3 years(p=0.512). Postoperative complications and the nal post-operative visual outcomes were similar between the groups.Conclusion: Subconjunctival Injection of MMC is as safe and effective as sponge application with comparable surgical outcomes and complications in the long term.Patients with uncontrolled glaucoma(both primary and secondary)either on maximal medical or manifesting a progression of visual eld loss were recruited for the study.Monocular patients,patients with a history of prior ocular surgeries,other ocular pathologies like active uveitis ,neovascularisation, suspected scleral thinning,patients with systemic comorbidities like connective tissue disorders, immunode ciency,pregnant or nursing women, and those unwilling to provide an informed consent were excluded.One eye of each eligible patient was included.