[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Gainesville Eye Associates\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":66},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,38],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":26,"lastUpdatePostDateStruct":27,"startDateStruct":30,"completionDateStruct":32,"leadSponsor":34,"locationsCount":37},"100641197","clareon-truplus-vs-tecnis-eyhance-iols-in-cataract-patients-100641197",false,"NCT07658040","Clareon TruPlus vs Tecnis Eyhance IOLs in Cataract Patients","Visual and Patient Reported Outcomes Comparing Clareon TruPlus IOL and Tecnis Eyhance IOLs in Normal Cataract Patients: Stage 1","Inclusion Criteria:\n\n* Willing and able to understand and sign informed consent.\n* Adult patient diagnosed with age-related cataracts bilaterally.\n* Planned bilateral cataract removal and with bilateral implantation of the Clareon TruPlus IOL\u002FToric BLF (T3-T5) or Tecnis Eyhance IOL\u002FEyhance Toric (equivalent to T3-T5).\n* Best monocular corrected distance visual acuity expected to be 0.1 logMAR (Snellen 20\u002F25) or better in both eyes postoperatively as determined by surgeon.\n* Residual astigmatism expected to be \\\u003C= 0.50 diopters in both eyes postoperatively as determined by surgeon (After using either toric IOL or arcuate incision with laser or manual LRI).\n* Normal ocular findings aside from cataract.\n\nExclusion Criteria:\n\n* Moderate-severe corneal pathology, irregular astigmatism, preexisting macular disease and other retinal degenerative diseases expected to cause future vision loss, glaucoma, severe dry eye disease, nystagmus, strabismus, zonular laxity or dehiscence, pseudoexfoliation.\n* Previous history of any ocular surgery including corneal refractive surgery.\n* History of amblyopia or monofixation syndrome with poor stereoscopic vision.\n* Participants desiring monovision.\n* Any planned simultaneous\u002Fcombined procedures at time of cataract surgery (e.g. MIGs).\n* Participation in another clinical study that could interfere with the results.\n* Any active ocular infection or inflammation.","ALL","18 Years",{"count":19,"type":20},70,"ESTIMATED","OBSERVATIONAL","This study is a prospective, randomized, two-arm, single-center, single-surgeon, double-masked (subject and assessor) comparative study. It involves bilateral implantation of intraocular lenses (IOLs), comparing Clareon TruPlus IOL and Tecnis Eyhance IOLs in normal cataract patients. The study will be conducted at one site and will include a pre-operative visit and a 3-month post-operative assessment.",[24],"Cataract","NOT_YET_RECRUITING","2026-06-16",{"date":28,"type":29},"2026-06-18","ACTUAL",{"date":31,"type":20},"2026-08-09",{"date":33,"type":20},"2027-08-09",{"name":35,"class":36},"Gainesville Eye Associates","OTHER",1,{"id":39,"slug":40,"hasResults":11,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":44,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":46,"targetDuration":4,"studyType":48,"phases":49,"briefSummary":51,"conditions":52,"keywords":54,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":37},"100617943","hud-surgical-guidance-for-toric-alignment-100617943","NCT07325188","HUD Surgical Guidance for Toric Alignment","Clinical Evaluation of a Novel Intraoperative Guidance System for Accurate Toric IOL Positioning in Cataract Surgery","CG-Toric","Inclusion criteria:\n\n* Patients undergoing uncomplicated cataract surgery with toric IOL implantation,\n* Eyes implanted with a toric IOL.\n\nExclusion criteria:\n\n* Ocular comorbidity likely to impair postoperative visual acuities, or\n* History of ocular trauma or zonular instability, or\n* Previous refractive surgery, or\n* Irregular corneal astigmatism or keratoconus, or\n* Patients with physical or intellectual disabilities that may prevent reliable fixation or comprehension (e.g. Down's Syndrome, Parkinson's Disease), or\n* Patients with unreliable biometry measurements, or\n* Severe dry eye disease or ocular surface disease.",{"count":47,"type":20},100,"INTERVENTIONAL",[50],"NA","This study aims to assess the accuracy of toric intraocular lens (IOL) alignment axes as calculated and displayed by a novel digital guidance system. In addition, it evaluates the time required to initiate surgical guidance and postoperative refractive astigmatism following toric IOL implantation.\n\nThis single-surgeon, single-site, prospective, non-invasive observational study evaluated the accuracy of toric IOL alignment axes calculated and displayed by the digital guidance system (Cassini Technologies, B.V.) in 100 eyes. The intraoperatively calculated alignment axes were compared to preoperative measurements to assess their accuracy (in degrees). Postoperative outcomes, including residual refractive astigmatism (diopters) and visual acuity (Snellen), were recorded at 1 month postoperatively.",[53],"Cataract and IOL Surgery",[55,56],"Guidance","Toric IOL","RECRUITING","2026-01-06",{"date":60,"type":29},"2026-01-08",{"date":62,"type":29},"2025-11-04",{"date":64,"type":20},"2026-10-31",{"name":35,"class":36},""]