Evidence map›Paper›PMID 28986670›Full record

Trial reportGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2018

Traumatic optic neuropathy treatment trial (TONTT): open label, phase 3, multicenter, semi-experimental trial.

Mohsen Bahmani Kashkouli, Sahar Yousefi, Marzieh Nojomi, Mostafa Soltan Sanjari, Farzad Pakdel, Morteza Entezari, Mohammad Etezad-Razavi, Mohammad Reza Razeghinejad, Manuchehr Esmaeli, Masoud Shafiee and 1 more

Registry-linked trialAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03308448 (Traumatic Optic Neuropathy Treatment Trial 2; Efficacy of Different Doses of Erythropoietin. A Multicenter, Double Blind RCT), which is not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.0field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03308448 phase3completednot on this map

Traumatic Optic Neuropathy Treatment Trial 2; Efficacy of Different Doses of Erythropoietin. A Multicenter, Double Blind RCT

TypeinterventionalSponsorIran University of Medical SciencesRan2018 to 2023Enrolled93ConditionsTraumatic Optic NeuropathyArmsRecombinant human erythropoietin
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 55 citations in OpenAlex.

  1. Combination of intravitreal bevacizumab and erythropoietin versus intravitreal bevacizumab alone for refractory diabetic macular edema: a randomized double-blind clinical trial.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2019
    Trial
  2. Factors affecting color vision: a systematic review.International journal of ophthalmology · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Traumatic Optic Neuropathy.Journal of neurological surgery. Part B, Skull base · 2021
    Article
  14. Isolated-check visual evoked potential: a more sensitive tool to detect traumatic optic neuropathy after orbital fracture.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2021
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Traumatic Optic Neuropathy.Korean journal of neurotrauma · 2018
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Mohsen Bahmani KashkouliEye Research Center, Rassoul Akram Hospital, Iran University of Medical Sciences, Sattarkhan-Niayesh St, Tehran, 14455-364, Iran. mkashkouli2@gmail.com.
Sahar YousefiEye Research Center, Rassoul Akram Hospital, Iran University of Medical Sciences, Sattarkhan-Niayesh St, Tehran, 14455-364, Iran.
Marzieh NojomiPreventive Medicine and Public Health Research Center, Department of Community Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mostafa Soltan SanjariEye Research Center, Rassoul Akram Hospital, Iran University of Medical Sciences, Sattarkhan-Niayesh St, Tehran, 14455-364, Iran.
Farzad PakdelEye Research Center, Rassoul Akram Hospital, Iran University of Medical Sciences, Sattarkhan-Niayesh St, Tehran, 14455-364, Iran.
Morteza EntezariEye Research Center, Imam Hossein Hospital, Beheshti University of Medical Sciences, Tehran, Iran.
Mohammad Etezad-RazaviEye Research Center, Khatam-al-anbia Hospital, Mashhad University of Medical Sciences, Mashhad, Iran.
Mohammad Reza RazeghinejadEye Research Center, Khalili Eye Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.
Manuchehr EsmaeliEye Research Center, Imam Hossein Hospital, Beheshti University of Medical Sciences, Tehran, Iran.
Masoud ShafieeEye Research Center, Khatam-al-anbia Hospital, Mashhad University of Medical Sciences, Mashhad, Iran.
Mansoureh BagheriEye Research Center, Khalili Eye Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.
Rasool Akram Hospital · IRImam Hossein Hospital · IRIran University of Medical Sciences · IRMashhad University of Medical Sciences · IRShiraz University of Medical Sciences · IR

Funding

Iran University Eye Research Center 90-01-124-12972
6 · The paper itself

Abstract

purposeIntravenously administered erythropoietin (EPO) was firstly commenced (phase 1) in patients with indirect traumatic optic neuropathy (TON) by this group in 2011. It was re-tested by another group (phase 2) in 2014. This multicenter clinical trial was designed to compare its effect with intravenous steroid and observation.

methodsIncluded were TON patients ≥5 years of age and with trauma-treatment interval of ≤3 weeks. Follow-up visits were set at 1, 2, 3, 7, 14, 30, and at least 90 days after treatment. EPO and methylprednisolone were infused intravenously every day for three consecutive days. Primary outcome measure was change in the best corrected visual acuity (BCVA). Secondary outcomes included change in color vision and relative afferent pupillary defect (RAPD), side effects, and factors affecting the final visual improvement.

resultsOut of 120 patients, 100 (EPO: 69, steroid: 15, observation: 16) were finally included. All three groups showed a significant improvement of BCVA which was not significantly different between the groups (adjusted for pretreatment BCVA). Color vision was significantly improved in the EPO group. Late treatment (>3 days) (odds ratio = 2.53) and initial BCVA of NLP (odds ratio = 5.74) significantly worsened visual recovery. No side effect was observed in any group.

conclusionEPO, steroid, and observation showed a significant improvement of BCVA in patients with TON. Initial BCVA of NLP and late treatment (>3 days) were significant risk factors for visual improvement.

Indexed as

Visual AcuityAdolescentAdultAgedChildChild, PreschoolColor VisionDose-Response Relationship, DrugErythropoietinFemaleGlucocorticoidsHumansInfusions, IntravenousMaleMethylprednisoloneMiddle AgedErythropoietinGlucocorticoidsMethylprednisoloneErythropoietinOptic neuropathyTrauma

Identifiers

PMID28986670
OpenAlexW2762171406

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.